Dayang Chem (Hangzhou) Co.,Ltd.
DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:947-91-1
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inquiryChemwill Asia Co., Ltd.
Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
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inquiryZhuozhou Wenxi import and Export Co., Ltd
WITH 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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inquiryHebei Sankai Chemical Technology Co., Ltd
1. Product advantages ♦ High purity, all above 98.5%, no impurities after dissolution ♦ We will test each batch to ensure quality ♦ OEM and private brand services designed for free ♦ Various cap colors available ♦ W
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inquiryHangzhou Sartort Biopharma Co., Ltd
Appearance:Colorless to yellow liquid Storage:Inert atmosphere,Store in freezer, under -20°C Package:200kg/Drum Application:Chemicals Transportation:Express/Sea/Air Port:Any port in China
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inquiryShanghai Upbio Tech Co.,Ltd
1.In No Less 10 years exporting experience. you 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 Specializ
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inquiryQingdao Beluga Import and Export Co., LTD
DIPHENYLACETALDEHYDE CAS:8947-91-1 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic inter
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inquiryShandong Hanjiang Chemical Co., Ltd.
Hello, 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
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inquiryHenan Wentao Chemical Product Co., Ltd.
Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Hangzhou J&H Chemical Co., Ltd.
J&H CHEM 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. J&H CHEM has some Manufacturing base in Jia
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inquiryZibo Hangyu Biotechnology Development Co., Ltd
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquiryHANGZHOU YUNUO CHEMICAL CO.,LTD
Superior quality, moderate price & quick delivery. Appearance:light yellow crystal powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:10g/bag，or as your request Application:Used as Pharmaceutical Intermed
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Min.Order:1 Gram
Negotiable
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inquiryHenan Tianfu Chemical Co., Ltd.
High Quality Best price Fast Delivery Good Service Welcome to Henan Tianfu Chemical Co., Ltd. website. Our company engages in Sodium Tripolyphosphate (STPP) and Sodium Hexametabphosphate (SHMP) production; developm
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inquiryHunan chemfish Pharmaceutical co.,Ltd
Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Kono Chem Co.,Ltd
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
GIHI CHEMICALS CO.,LIMITED
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
Hangzhou Dingyan Chem Co., Ltd
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Shanghai Acmec Biochemical Technology Co., Ltd.
Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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Min.Order:1 bottle
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inquiryHenan Allgreen Chemical Co.,Ltd
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Chemsigma International Co.,Ltd.
bulk productiongoods in stockswe have the best competitive price in the marketmeantime,we are committed to service to our every customer Chemsigma International Co.,Ltd. is a chemical manufacturer, specialize in custom synthesis and organic chemical
Antimex Chemical Limied
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryHangzhou Fandachem Co.,Ltd
Benzeneacetaldehyde, a-phenyl- cas 947-91-1Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
Henan Kanbei Chemical Co.,LTD
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Shanghai Chinqesen Biotechnology Co., Ltd.
Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
Hubei Jiutian Bio-medical Technology Co., Ltd
Trimeric sodium phosphate detergent auxiliary agent is a kind of excellent properties, is one of the biggest component of detergent consumption during the production, it has four aspects: 1, chelation of heavy metal ions, heavy metal ions in the wate
Chemlyte Solutions
Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Synthetic route
| Conditions | Yield |
|---|---|
| With C36H54IrNP(1+)*C32H12BF24(1-) In tetrahydrofuran at 23 - 100℃; for 24h; Schlenk technique; Inert atmosphere; Sealed tube; | 99% |
| With rhenium(I) pentacarbonyl bromide In monoethylene glycol diethyl ether at 80℃; for 1h; Meinwald Rearrangement; Inert atmosphere; chemoselective reaction; | 93% |
| With indium(III) chloride In tetrahydrofuran at 25℃; for 0.25h; Rearrangement; | 90% |
| Conditions | Yield |
|---|---|
| With erbium(III) triflate In dichloromethane at 20℃; for 0.75h; | 99% |
| With trimethylaluminum; 1,3-bis(3-t-butyl-5-methylsalicyl)benzene In dichloromethane Ambient temperature; | 98% |
| With copper(II) tetrafluoroborate hydrate In dichloromethane for 1.5h; Meinwald rearrangement; Reflux; regioselective reaction; | 95% |
| Conditions | Yield |
|---|---|
| With diethylzinc; trifluoroacetic acid In dichloromethane at 0℃; for 0.166667h; Inert atmosphere; | 99% |
-
-
492-70-6, 655-48-1, 2325-10-2, 38270-73-4, 52340-78-0, 579-43-1
1,2-diphenyl-1,2-ethanediol
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With KSF clay Irradiation; microwave irradiation; | 98% |
| With poly(3,4-ethylenedioxythiophene) In toluene Reflux; Inert atmosphere; | 88% |
| With USY-6 molecular sieve In toluene at 110℃; for 5h; Pinacol Rearrangement; | 88.6% |
-
-
58176-63-9
1,2-diphenyl-2-methoxyethanol
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With hydrogenchloride; trifluoroacetic acid at 70℃; for 0.666667h; | 98% |
| Conditions | Yield |
|---|---|
| With gold(III) chloride; silver hexafluoroantimonate In 1,4-dioxane at 20℃; for 0.0833333h; regioselective reaction; | 98% |
| With methylaluminium bis(4-bromo-2,6-di-tert.-butylphenoxide) In dichloromethane at -20℃; for 0.3h; | 95% |
| copper(I) tetrafluoroborate In dichloromethane for 1.5h; Meinwald rearrangement reaction; Heating; | 95% |
| With bismuth(lll) trifluoromethanesulfonate at 20℃; for 0.0833333h; Reagent/catalyst; Time; Schlenk technique; Sonication; Ionic liquid; Green chemistry; regioselective reaction; | 80% |
| With mesoporous silica-supported Er(III) catalyst In toluene at 100℃; for 4h; |
| Conditions | Yield |
|---|---|
| With 9-borabicyclo[3.3.1]nonane dimer In tetrahydrofuran for 1h; Ambient temperature; | 98% |
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With 9-borabicyclo[3.3.1]nonane dimer In tetrahydrofuran for 1h; Ambient temperature; | 98% |
| Conditions | Yield |
|---|---|
| cyclopentadienyldicarbonyl(tetrahydrofuran)iron(II) tetrafluoroborate In dichloromethane-d2 for 3h; Isomerization; | 98% |
| With <(η5-C5H5)Fe(CO)2(THF)>+- In dichloromethane for 3h; Ambient temperature; | 93% |
| With bismuth oxide perchlorate In dichloromethane at 20℃; for 0.416667h; Rearrangement; | 90% |
| Conditions | Yield |
|---|---|
| With gold(III) chloride; silver hexafluoroantimonate In 1,4-dioxane at 20℃; for 0.0833333h; regioselective reaction; | A 11 %Spectr. B 98% |
| With (5,10,15,20-tetraphenylporphyrinato-κ4N)(trifluoromethylsulfonate)iron(III) In 1,2-dichloro-ethane at 83℃; for 1h; Inert atmosphere; | A 23% B 73% |
| With bismuth(lll) trifluoromethanesulfonate In dichloromethane for 0.5h; | A n/a B 92 % Spectr. |
| Conditions | Yield |
|---|---|
| With 9-borabicyclo[3.3.1]nonane dimer; lithium dihydrido borata-bicyclo[3.3.0]nonane In tetrahydrofuran for 6h; Ambient temperature; | 96% |
| With thexylchloroborane-Me2SO4 In dichloromethane for 0.25h; Ambient temperature; | 91% |
| With thexylbromoborane dimethyl sulfide complex In carbon disulfide; dichloromethane at -20 - 20℃; for 1h; | 89% |
-
-
1689-71-0, 17619-97-5, 25144-18-7, 38628-70-5, 40102-60-1, 1439-07-2
2,3-diphenyloxirane
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| methylaluminium bis(4-bromo-2,6-di-tert.-butylphenoxide) In dichloromethane at -20℃; for 0.3h; | 95% |
| With [5,10,15,20-tetraphenylporphinato]ytterbium(III) triflate In α,α,α-trifluorotoluene at 102℃; for 3h; Inert atmosphere; regioselective reaction; | 91% |
| In hexane Ambient temperature; rearrangement on immobilized monomethylaluminum bis(4-bromo-2,6-diphenylphenoxide) column; | 72% |
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With sodium carbonate In water | 95% |
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With Cr-pillared montmorillonite In tetrahydrofuran for 4h; Time; Reflux; regioselective reaction; | 92% |
| With rhenium(I) pentacarbonyl bromide In monoethylene glycol diethyl ether at 80℃; for 5h; Reagent/catalyst; Solvent; Temperature; Time; Meinwald Rearrangement; Inert atmosphere; | 72% |
| Conditions | Yield |
|---|---|
| In chloroform for 1h; | 91% |
| With scandium tris(trifluoromethanesulfonate) In toluene at -20℃; for 0.166667h; Inert atmosphere; | 79% |
| Conditions | Yield |
|---|---|
| With polymer(resin Amberlyst A-26)-supported tetracarbonylhydridoferrate anion In tetrahydrofuran for 1h; Heating; | 90% |
| With tri-n-butyl-tin hydride; tetrakis(triphenylphosphine) palladium(0) In benzene for 0.166667h; Ambient temperature; | 75% |
| With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium tetrahydroborate; cadmium(II) chloride In acetonitrile at -5℃; for 0.05h; | |
| Multi-step reaction with 2 steps 1: triethylsilane; triethylamine / tetrahydrofuran / 1 h / 20 °C 2: triethylsilane / tetrahydrofuran / 1 h View Scheme |
| Conditions | Yield |
|---|---|
| With hydrogenchloride In acetic acid for 0.166667h; Heating; | 90% |
| Conditions | Yield |
|---|---|
| With phenylsilane; cobalt(II) diacetate tetrahydrate; sodium triethylborohydride In 1,2-dimethoxyethane; toluene at 25℃; for 15h; Inert atmosphere; Schlenk technique; | 90% |
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With sodium carbonate In water | 89% |
| Conditions | Yield |
|---|---|
| With nanoporous aluminosilicate (Al-13-(3.18)) at 40℃; for 3h; Reagent/catalyst; Meinwald Rearrangement; | A n/a B 88% |
| With bismuth(lll) trifluoromethanesulfonate In dichloromethane for 0.333333h; | A n/a B 92 % Spectr. |
-
-
3277-26-7
1,1,3,3-Tetramethyldisiloxane
-
-
117-34-0
2,2-diphenylacetic acid
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| Stage #1: 1,1,3,3-Tetramethyldisiloxane; 2,2-diphenylacetic acid With C24H23ClCrIrNO3; sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate In dichloromethane at 40℃; for 15h; Schlenk technique; Glovebox; Inert atmosphere; Stage #2: With water In dichloromethane at 25℃; for 1h; | 88% |
-
-
36586-15-9
(2-ethoxyethene-1,1-diyl)dibenzene
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With trifluoroacetic acid In dichloromethane at 20℃; for 1h; | 85% |
| With hydrogenchloride; acetic acid |
| Conditions | Yield |
|---|---|
| With titanium(IV) isopropylate; 1,1,3,3-Tetramethyldisiloxane In toluene at 20℃; for 48h; Inert atmosphere; | 85% |
-
-
78108-69-7
2-(2,2-Diphenyl-vinyl)-1,1,3,3-tetramethyl-2,3-dihydro-1H-benzo[1,2,5]azadisilole
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With hydrogenchloride | 84% |
-
-
1689-71-0, 17619-97-5, 25144-18-7, 38628-70-5, 40102-60-1, 1439-07-2
2,3-diphenyloxirane
-
A
-
947-91-1
Diphenylacetaldehyde
-
B
-
103-30-0
(E)-1,2-diphenyl-ethene
| Conditions | Yield |
|---|---|
| With molybdenum hexacarbonyl In benzene for 3h; Heating; | A 14% B 84% |
| With molybdenum hexacarbonyl In 1,2-dimethoxyethane Heating; | A 66% B 28% |
| Conditions | Yield |
|---|---|
| Stage #1: 1,1-Diphenylethylene for 0.05h; Inert atmosphere; Stage #2: With tert.-butylhydroperoxide at 102℃; for 6h; Inert atmosphere; | 80% |
| With chloropyridinecobaloxime(III); water; 9-(2-mesityl)-10-methylacridinium perchlorate In acetonitrile at 20℃; for 24h; Wacker Oxidation; Inert atmosphere; Schlenk technique; Irradiation; | 68% |
| With Perbenzoic acid; chloroform at 0 - 5℃; |
| Conditions | Yield |
|---|---|
| With iodobenzene complex with boron trifluoride etherate In dichloromethane at -10℃; | 80% |
| With hypoiodous acid; acetone at -40 - 20℃; | |
| Multi-step reaction with 2 steps 1: 92 percent / m-chloroperbenzoic acid / diethyl ether / Ambient temperature 2: 28 percent / PdCl2(MeCN)2, CuCl2, air / CH2Cl2 / 15 h / Ambient temperature; Irradiation View Scheme |
-
-
645-49-8
cis-stilben
-
A
-
947-91-1
Diphenylacetaldehyde
-
B
-
103-30-0
(E)-1,2-diphenyl-ethene
-
C
-
100-52-7
benzaldehyde
| Conditions | Yield |
|---|---|
| 2,4,6-triphenylpyrylium tetrafluoroborate for 4h; Product distribution; Irradiation; | A 7% B 80% C 12% |
| Conditions | Yield |
|---|---|
| With hydrogenchloride; tin(ll) chloride In acetic acid for 0.05h; Heating; | 80% |
| Multi-step reaction with 2 steps 1: amalgamated aluminium; diethyl ether 2: concentrated hydrochloric acid; glacial acetic acid View Scheme |
-
-
947-91-1
Diphenylacetaldehyde
-
-
204258-62-8
((S)-2-Hydroxy-1-phenyl-ethylamino)-acetic acid methyl ester
-
-
204258-63-9
((2S,4S)-2-Benzhydryl-4-phenyl-oxazolidin-3-yl)-acetic acid methyl ester
| Conditions | Yield |
|---|---|
| With magnesium sulfate In dichloromethane for 12h; Ambient temperature; | 100% |
| Conditions | Yield |
|---|---|
| With toluene-4-sulfonic acid In toluene Heating; | 100% |
| Conditions | Yield |
|---|---|
| With n-butyllithium; N,N,N,N,-tetramethylethylenediamine In tetrahydrofuran at -78 - 20℃; for 2h; | 100% |
| Conditions | Yield |
|---|---|
| In tetrahydrofuran at 20℃; for 0.5h; | 100% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
133658-80-7
2-cyclopentyl-2-phenylethen-1-one
-
-
865363-46-8
(S)-Cyclopentyl-phenyl-acetic acid 2,2-diphenyl-vinyl ester
| Conditions | Yield |
|---|---|
| With chiral (-)-ferrocene catalyst In chloroform at 0℃; for 22h; | 99% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
133658-80-7
2-cyclopentyl-2-phenylethen-1-one
-
-
865363-56-0
(R)-Cyclopentyl-phenyl-acetic acid 2,2-diphenyl-vinyl ester
| Conditions | Yield |
|---|---|
| With chiral (+)-ferrocene catalyst In chloroform at 0℃; for 22h; | 99% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
463299-70-9
2-(o-tolyl)but-1-en-1-one
-
-
865363-58-2
2-o-tolyl-butyric acid 2,2-diphenyl-vinyl ester
| Conditions | Yield |
|---|---|
| With chiral (+)-ferrocene catalyst In chloroform at 0℃; for 22h; | 99% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
463299-70-9
2-(o-tolyl)but-1-en-1-one
-
-
865363-48-0
2-o-tolyl-butyric acid 2,2-diphenyl-vinyl ester
| Conditions | Yield |
|---|---|
| With chiral (-)-ferrocene catalyst In chloroform at 0℃; for 22h; | 99% |
-
-
615-06-5
3-furan-2-yl-3-oxo-propionic acid methyl ester
-
-
947-91-1
Diphenylacetaldehyde
-
-
1272565-10-2
C22H18O4
| Conditions | Yield |
|---|---|
| With piperidine; acetic acid In benzene at 100℃; for 16h; Knoevenagel condensation; Inert atmosphere; optical yield given as %de; | 99% |
| Conditions | Yield |
|---|---|
| Stage #1: Diphenylacetaldehyde With [(N,N'-bis(diisopropylphosphino)-2,6-diaminopyridine)Mn(CO)2H] In 1,2-dimethoxyethane at 110℃; for 18h; Inert atmosphere; Sealed tube; Stage #2: With sodium hydroxide at 25℃; for 18h; Inert atmosphere; chemoselective reaction; | 98% |
| With iron(II) fluoro{tris[2-(diphenylphosphino)phenyl]phospino}tetrafluoroborate; hydrogen; trifluoroacetic acid In isopropyl alcohol at 120℃; under 15001.5 Torr; for 2h; Inert atmosphere; Autoclave; chemoselective reaction; | 95% |
| With lithium aluminium tetrahydride In diethyl ether for 2h; Heating; | 90% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
87-51-4
indole-3-acetic acid
-
-
1167437-76-4
2-(1-(2,2-diphenylvinyl)-1H-indol-3-yl)acetic acid
| Conditions | Yield |
|---|---|
| Stage #1: Diphenylacetaldehyde; indole-3-acetic acid With trifluoroacetic acid In acetonitrile at 140℃; for 1h; Inert atmosphere; Microwave irradiation; Stage #2: With sodium hydrogencarbonate In water; ethyl acetate; acetonitrile | 98% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
5351-23-5
4-hydroxybenzoic acid hydrazide
-
-
386283-90-5
diphenylacetaldehyde p-hydroxybenzoylhydrazone
| Conditions | Yield |
|---|---|
| With acetic acid In ethanol for 4h; Reflux; | 98% |
-
-
947689-42-1
N-(2-iodophenyl)-4-methyl-N-(propa-1,2-dien-1-yl)benzenesulfonamide
-
-
947-91-1
Diphenylacetaldehyde
| Conditions | Yield |
|---|---|
| With tetrakis(triphenylphosphine) palladium(0); Benzhydrylamine; sodium t-butanolate In tetrahydrofuran at 50℃; for 8h; Inert atmosphere; Sealed tube; | 98% |
| Conditions | Yield |
|---|---|
| With tetrakis(triphenylphosphine) palladium(0); benzoic acid In 1,4-dioxane at 100℃; for 15h; | 97% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
75-64-9
tert-butylamine
-
-
55103-28-1
1-tert.-Butylamino-2,2-diphenylethylen
| Conditions | Yield |
|---|---|
| With magnesium sulfate In dichloromethane for 1h; Heating; | 96% |
-
-
109-80-8
1.3-propanedithiol
-
-
947-91-1
Diphenylacetaldehyde
-
-
34399-66-1
2-(diphenylmethyl)-1,3-dithiane
| Conditions | Yield |
|---|---|
| With 4 A molecular sieve; boron trifluoride diethyl etherate In dichloromethane Condensation; | 96% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
126899-77-2
1,1-diphenyl-3-butene-1-carboxaldehyde
| Conditions | Yield |
|---|---|
| With ionic liquid; phosphine ligand; triethylamine; palladium catalyst at 20℃; for 5h; | 96% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
4124-41-8
p-toluenesulfonylanhydride
-
-
102478-11-5
2,2-diphenylvinyl 4-methylbenzenesulfonate
| Conditions | Yield |
|---|---|
| Stage #1: Diphenylacetaldehyde With sodium t-butanolate In tetrahydrofuran at -20 - 20℃; for 1.5h; Inert atmosphere; Stage #2: p-toluenesulfonylanhydride In tetrahydrofuran at -15 - -5℃; for 1.5h; Inert atmosphere; | 96% |
| Stage #1: Diphenylacetaldehyde With sodium t-butanolate In tetrahydrofuran at -20 - 20℃; Inert atmosphere; Stage #2: p-toluenesulfonylanhydride In tetrahydrofuran at -15 - -5℃; for 1.5h; Inert atmosphere; | 96% |
-
-
947-91-1
Diphenylacetaldehyde
-
-
3471-31-6
5-methoxy-1H-indole-3-acetic acid
-
-
1167437-79-7
2-(5-methoxy-1-(2,2-diphenylvinyl)-1H-indol-3-yl)acetic acid
| Conditions | Yield |
|---|---|
| Stage #1: Diphenylacetaldehyde; 5-methoxy-1H-indole-3-acetic acid With trifluoroacetic acid In acetonitrile at 140℃; for 1h; Inert atmosphere; Microwave irradiation; Stage #2: With sodium hydrogencarbonate In water; ethyl acetate; acetonitrile | 96% |
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