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Cas:174501-64-5
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
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inquiryDayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
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inquiryFactory supply 1-Butyl-3-methylimidazolium hexafluorophosphate CAS 174501-64-5 with fast delivery Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical &
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inquiryThe company has a professional R & D team, mature technology, very competitive prices and stable high quality products for customers to order high quality and low price product efforts! Appearance:White or off-white Solid Storage:Sealed, dr
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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inquiryName 1-But
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inquiryTIANFUCHEM--174501-64-5--1-Butyl-3-methylimidazolium hexafluorophosphate factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had est
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryName 1-Butyl-3-methylimidazolium hexafluorophosphate/BMIMPF6 CAS NO. 174501-64-5 Molecular Formula C8H15N2.PF6 Molecular Weight 284.18
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Cas:174501-64-5
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inquiryOur Advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We
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inquiryAppearance:Colorless or Pale yellow liquid Storage:ln stock Package:25kg/Barrel Application:ionic liquid Transportation:Express/Sea/Air Port:Any port of China
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inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
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inquiryWe are the manufacturers and suppliers of API in China, and warehouse in Germany and USA of California, which can quickly and safely deliver to your address 1.High quality and competitive price. 2.Free sample for your evaluation. 3.Promptly delivery
Cas:174501-64-5
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inquiryPacking: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once Appearance:Clear colorless liquid Storage:Refer to COA / M
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inquiryOur company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present,
Cas:174501-64-5
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Cas:174501-64-5
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inquiry1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highly qualifie
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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
Cas:174501-64-5
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inquiryHunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
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Cas:174501-64-5
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inquiryEstablished in May 2015, TaiChem Ltd. is initially invested by a British research and development company and started by PhDs back from aboard. The company is registered in China Medical City (CMC), Taizhou, Jiangsu Province, and the production site
Cas:174501-64-5
Min.Order:10 Gram
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inquiryProduct name: 1-Butyl-3-Methylimidazolium Hexafluorophosphate CAS No.:174501-64-5 Molecule Formula:C8H16F6N2P Molecule Weight:285.19 Purity: 99.0% Package: 200kg/drum Description:Yellow liquid Manufacture Standards:Enterprise Standard
Cas:174501-64-5
Min.Order:1 Kilogram
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inquiryWe are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
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Cas:174501-64-5
Min.Order:10 Gram
Negotiable
Type:Other
inquiry1-butyl-3-methylimidazolium chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With Amberlyst A-26 (PF6- form) In methanol | 100% |
With sodium hexaflorophosphate In acetone at 80℃; for 0.166667h; microwave irrradiation; | 99% |
With potassium hexafluorophosphate In acetone at 20℃; for 24h; | 98% |
1-n-butyl-3-methylimidazolim bromide
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate In water at 20℃; | 100% |
With ammonium hexafluorophosphate In water at 20℃; for 2h; | 91% |
With potassium hexafluorophosphate In water at 20℃; for 24h; | 87% |
1-methyl-3-(n-butyl)imidazolium iodide
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With Amberlyst A-26 (PF6- form) In methanol | 100% |
With Amberlist A-26 BF6(-) form In methanol Ionic liquid; |
1-Butylimidazole
trimethyl orthoformate
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With ammonium hexafluorophosphate Reagent/catalyst; Schlenk technique; Reflux; | 95% |
With ammonium hexafluorophosphate at 110℃; for 17h; Reagent/catalyst; Inert atmosphere; | 88% |
1-methyl-1H-imidazole
1-bromo-butane
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate at 40 - 120℃; for 0.166667h; microwave irradiation; sonication; | 94% |
With potassium hexafluorophosphate at 80℃; for 3.5h; | 93% |
With ammonium hexafluorophosphate; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 80℃; for 15h; | 89% |
1-methyl-1H-imidazole
n-Butyl chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With sodium hexaflorophosphate at 70℃; for 336h; | 92% |
Stage #1: 1-methyl-1H-imidazole; n-Butyl chloride In toluene for 48h; Reflux; Stage #2: With potassium hexafluorophosphate In toluene | 92% |
With potassium hexafluorophosphate at 120 - 180℃; for 0.75h; microwave irradiation; | 90% |
1-Butylimidazole
dimethyl sulfate
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: 1-Butylimidazole; dimethyl sulfate for 0.25h; Stage #2: With sodium hexaflorophosphate In water | 92% |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate In acetone for 24h; | 90% |
methanol
N-methyl-N'-n-butylimidazolium-2-carboxylate
A
potassium monomethylcarbonate
B
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate at 20℃; for 12h; | A 87% B 72% |
1-methyl-1H-imidazole
1-iodo-butane
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 80℃; for 10h; | 85% |
1-n-butyl-3-methylimidazolim bromide
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 24h; | 75% |
Trimethyl borate
hydrogen fluoride
1-butyl-3-methylimidazolium chloride
D
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: potassium fluoride; N-trimethylsilyl-tris(pentafluorethyl)phosphazen; Trimethyl borate In 1,2-dimethoxyethane at 20 - 60℃; for 1h; Stage #2: hydrogen fluoride In 1,2-dimethoxyethane; water at 0 - 20℃; for 3h; Stage #3: 1-butyl-3-methylimidazolium chloride In water | A 60% B 30% C 6% D 4% |
1-Butylimidazole
carbonic acid dimethyl ester
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: 1-Butylimidazole; carbonic acid dimethyl ester In methanol at 135℃; for 7h; Stage #2: With sodium hexaflorophosphate In methanol; acetone at 25℃; for 2h; | 52% |
1-Butylimidazole
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 60 - 70 °C 2: NH4PF6 View Scheme |
1-butyl-3-methylimidazolium chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
at 20℃; |
formaldehyd
Glyoxal
N-butylamine
methylamine
A
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: formaldehyd; N-butylamine; methylamine In water at 0℃; Stage #2: With hexafluorophosphoric acid In water at 0℃; Stage #3: Glyoxal In water at 0 - 20℃; |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With sodium hexaflorophosphate |
1-methyl-1H-imidazole
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With alkali metal hexafluorophosphate at 150℃; for 0.5h; Microwave irradiation; Cooling; neat (no solvent); |
potassium hexafluorophosphate
1-butyl-3-methylimidazolium chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In water at 20℃; for 24h; |
1-butyl-3-methylimidazolium chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In water | |
Ionic liquid; Inert atmosphere; |
1-butyl-3-methylimidazolium chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With Amberlyst A-26 (PF6- form) In methanol | 100% |
With sodium hexaflorophosphate In acetone at 80℃; for 0.166667h; microwave irrradiation; | 99% |
With potassium hexafluorophosphate In acetone at 20℃; for 24h; | 98% |
1-n-butyl-3-methylimidazolim bromide
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate In water at 20℃; | 100% |
With ammonium hexafluorophosphate In water at 20℃; for 2h; | 91% |
With potassium hexafluorophosphate In water at 20℃; for 24h; | 87% |
1-methyl-3-(n-butyl)imidazolium iodide
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With Amberlyst A-26 (PF6- form) In methanol | 100% |
With Amberlist A-26 BF6(-) form In methanol Ionic liquid; |
1-Butylimidazole
trimethyl orthoformate
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With ammonium hexafluorophosphate Reagent/catalyst; Schlenk technique; Reflux; | 95% |
With ammonium hexafluorophosphate at 110℃; for 17h; Reagent/catalyst; Inert atmosphere; | 88% |
1-methyl-1H-imidazole
1-bromo-butane
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate at 40 - 120℃; for 0.166667h; microwave irradiation; sonication; | 94% |
With potassium hexafluorophosphate at 80℃; for 3.5h; | 93% |
With ammonium hexafluorophosphate; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 80℃; for 15h; | 89% |
1-methyl-1H-imidazole
n-Butyl chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With sodium hexaflorophosphate at 70℃; for 336h; | 92% |
Stage #1: 1-methyl-1H-imidazole; n-Butyl chloride In toluene for 48h; Reflux; Stage #2: With potassium hexafluorophosphate In toluene | 92% |
With potassium hexafluorophosphate at 120 - 180℃; for 0.75h; microwave irradiation; | 90% |
1-Butylimidazole
dimethyl sulfate
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: 1-Butylimidazole; dimethyl sulfate for 0.25h; Stage #2: With sodium hexaflorophosphate In water | 92% |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate In acetone for 24h; | 90% |
methanol
N-methyl-N'-n-butylimidazolium-2-carboxylate
A
potassium monomethylcarbonate
B
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate at 20℃; for 12h; | A 87% B 72% |
1-methyl-1H-imidazole
1-iodo-butane
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With potassium hexafluorophosphate; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 80℃; for 10h; | 85% |
1-n-butyl-3-methylimidazolim bromide
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 24h; | 75% |
Trimethyl borate
hydrogen fluoride
1-butyl-3-methylimidazolium chloride
D
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: potassium fluoride; N-trimethylsilyl-tris(pentafluorethyl)phosphazen; Trimethyl borate In 1,2-dimethoxyethane at 20 - 60℃; for 1h; Stage #2: hydrogen fluoride In 1,2-dimethoxyethane; water at 0 - 20℃; for 3h; Stage #3: 1-butyl-3-methylimidazolium chloride In water | A 60% B 30% C 6% D 4% |
1-Butylimidazole
carbonic acid dimethyl ester
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: 1-Butylimidazole; carbonic acid dimethyl ester In methanol at 135℃; for 7h; Stage #2: With sodium hexaflorophosphate In methanol; acetone at 25℃; for 2h; | 52% |
1-Butylimidazole
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 60 - 70 °C 2: NH4PF6 View Scheme |
1-butyl-3-methylimidazolium chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
at 20℃; |
formaldehyd
Glyoxal
N-butylamine
methylamine
A
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: formaldehyd; N-butylamine; methylamine In water at 0℃; Stage #2: With hexafluorophosphoric acid In water at 0℃; Stage #3: Glyoxal In water at 0 - 20℃; |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With sodium hexaflorophosphate |
1-methyl-1H-imidazole
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With alkali metal hexafluorophosphate at 150℃; for 0.5h; Microwave irradiation; Cooling; neat (no solvent); |
potassium hexafluorophosphate
1-butyl-3-methylimidazolium chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In water at 20℃; for 24h; |
1-butyl-3-methylimidazolium chloride
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In water | |
Ionic liquid; Inert atmosphere; |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
1-butyl-3-methylimidazolium chloride
Conditions | Yield |
---|---|
With Amberlyst A-26 (Cl- form) In methanol | 100% |
3,6-bis-(3,5-dimethyl-pyrazol-1-yl)-1,2,4,5-tetrazine
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate With potassium carbonate In acetonitrile for 0.666667h; Heating; Stage #2: 3,6-bis-(3,5-dimethyl-pyrazol-1-yl)-1,2,4,5-tetrazine In acetonitrile Heating; Further stages.; | 99% |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
1-butyl-3-methyl-1H-imidazole-2(3H)-thione
Conditions | Yield |
---|---|
Stage #1: 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 20℃; Electrolysis; Inert atmosphere; Stage #2: With sulfur for 0.166667h; Inert atmosphere; Irradiation; | 99% |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
1-butyl-3-methyl-2-imidazolone
Conditions | Yield |
---|---|
With superoxide radical anion at 25℃; under 742.574 Torr; Kinetics; Inert atmosphere; | 95% |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In toluene byproducts: H2O; Au complex and (C3H3N2(CH3)C4H9)PF6 added to toluene, stirred at 25°C for 14 h; pptd. (pentane), collected on a frit, washed (pentane), dried (vac.); elem. anal.; | 95% |
chloro-diphenylphosphine
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate With n-butyllithium In tetrahydrofuran; hexane at -20℃; for 0.75h; Metallation; Stage #2: chloro-diphenylphosphine In tetrahydrofuran; hexane at -78℃; for 0.166667h; Substitution; | 89% |
Stage #1: 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate With n-butyllithium In hexane; dichloromethane at -78℃; for 1h; Stage #2: chloro-diphenylphosphine In hexane; dichloromethane at -78 - 20℃; | 88% |
With n-butyllithium In hexane; dichloromethane at -78℃; for 1.08333h; | 84% |
4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
With NaOH In ethanol; water (N2) soln. 1M NaOH was added to soln. ligand in EtOH at room temp., EuCl3*6H2O was added, stirred for 4 h at 50°C, evapd., residue was washed with hexane, dissolved in water, soln. (C4mim)Br in aq. EtOH was added, stirred for 1 h at room temp.; ppt. was filtered, washed with hexane, dried under vac.; elem. anal.; | 77% |
carbon disulfide
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate With potassium tert-butylate In tetrahydrofuran at 20℃; for 0.25h; Inert atmosphere; Stage #2: carbon disulfide In tetrahydrofuran at 20℃; for 0.5h; Mechanism; Inert atmosphere; | 76% |
acetylacetone
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
Stage #1: acetylacetone With sodium hydroxide In ethanol; water pH=8; Stage #2: 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate In ethanol; water at 50℃; for 0.5h; Stage #3: terbium(III) nitrate pentahydrate In ethanol; water at 50℃; for 2h; | 72% |
carbon dioxide
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
N-methyl-N'-n-butylimidazolium-2-carboxylate
Conditions | Yield |
---|---|
With potassium tert-butylate In N,N-dimethyl-formamide at 100℃; under 60006 Torr; for 12h; Autoclave; | 70% |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In acetonitrile Inert atmosphere; Glovebox; Schlenk technique; | 41% |
1-methyl-1H-imidazole
iron pentacarbonyl
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In further solvent(s) byproducts: CO; Sonication; Fe complex and ligand dispersed in ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate, conicated at 40-50°C for 30 min (air); pptd.(ethanol), elem. anal., XRD; | 28% |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
1-n-butyl-3-methyl-2,3-dihydro-imidazol-2-ylidene
Conditions | Yield |
---|---|
With n-butyllithium In hexane; dichloromethane at -78℃; for 1h; | |
With N,N,N,N-tetraethylammonium tetrafluoroborate In N,N-dimethyl-formamide at 25℃; Inert atmosphere; Electrolysis; | |
In N,N-dimethyl-formamide at 25℃; Inert atmosphere; Electrolysis; |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
A
1-methyl-1H-imidazole
B
1-butylene
C
1-fluorobutane
Conditions | Yield |
---|---|
With cesium fluoride at 150℃; for 96h; |
furfural
acrylic acid methyl ester
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
A
methyl 2-(furan-2-yl(hydroxy)methyl)acrylate
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane at 20℃; for 24h; Baylis-Hillman; |
3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate
Conditions | Yield |
---|---|
In water; acetonitrile Radiolysis; |
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