CAS No.13326-10-8,Benzyl methyl carbonate Suppliers

Qingdao Beluga Import and Export Co., LTD

Benzyl Methyl Carbonate CAS:13326-10-8 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 i

Benzyl Methyl Carbonate CAS:13326-10-8

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Shandong Hanjiang Chemical Co., Ltd.

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Henan 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

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Zibo Hangyu Biotechnology Development Co., Ltd

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Xi`an Eastling Biotech Co., Ltd.

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou

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Henan Tianfu Chemical Co., Ltd.

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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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Hangzhou Sartort Biopharma Co., Ltd

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Henan Kanbei Chemical Co.,LTD

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ZHEJIANG JIUZHOU CHEM CO.,LTD

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Shanghai united Scientific Co.,Ltd.

United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat

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Nanjing Raymon Biotech Co., Ltd.

Benzyl methyl carbonateAppearance:Off white to slight yellow solid Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL

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Skyrun Industrial Co.,Ltd

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Benzyl methyl carbonateAppearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Protect the

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Synthetic route

: 616-38-6
carbonic acid dimethyl ester

: 100-51-6
benzyl alcohol

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
Stage #1: carbonic acid dimethyl ester With lanthanum(III) isopropoxide; 2-(2-methoxyethoxy)ethyl alcohol at 20℃; Stage #2: benzyl alcohol for 1h; Reflux; chemoselective reaction;	99%
With lanthanum (III) nitrate * water; 1,1,1-trioctyl-1-methylphosphonium methylcarbonate for 1h; Molecular sieve; Reflux;	99%
With 3-methyl-1-(trimethoxysilylpropyl)imidazolium chloride at 80℃; for 5h; Inert atmosphere;	99%

: 79-22-1
methyl chloroformate

: 100-51-6
benzyl alcohol

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
With pyridine In dichloromethane at 0 - 20℃;	97%
With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide In dichloromethane; water at 20℃; Inert atmosphere;	91%
With pyridine In dichloromethane at 0 - 20℃; Inert atmosphere;	90%

: 67-56-1
methanol

: C15H18N4O3

A: BrH*C7H11BrN4O

B: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
With bromine at 12℃; for 0h; Inert atmosphere; Darkness;	A 97% B 95%

...Expand

: 14660-45-8
potassium monomethylcarbonate

: 100-44-7
benzyl chloride

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
With 18-crown-6 ether In toluene Heating;	95%

: 100477-67-6
silver monomethyl carbonate

: 100-39-0
benzyl bromide

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
In acetonitrile at 25℃; for 10h;	91%

: 100-39-0
benzyl bromide

: tetra-n-butylammonium methyl carbonate

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
In acetonitrile at 25℃; for 18h;	86%

: 616-38-6
carbonic acid dimethyl ester

: 100-51-6
benzyl alcohol

A: 3459-92-5
DBC

B: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
ytterbium(III) triflate In 1,2-dichloro-ethane for 8h; Heating;	A n/a B 75%
ytterbium(III) triflate In 1,2-dichloro-ethane for 8h; Heating;	A 60% B 11%
With tungsten hexacarbonyl at 180℃; for 1h;	A 50% B n/a

...Expand

: 2-methoxycarbonyl-1,3-dimethylimidazolium triflate

: 100-51-6
benzyl alcohol

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane In acetone Ambient temperature;	74%
With 1,4-diaza-bicyclo[2.2.2]octane In acetone Product distribution; Mechanism; Ambient temperature; further alkyl imidazolium-2-carboxylates, further nucleophiles;	74%

: 616-38-6
carbonic acid dimethyl ester

: 100-51-6
benzyl alcohol

A: 3459-92-5
DBC

B: 103-50-4
dibenzyl ether

C: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
at 90℃; for 6h; Reagent/catalyst; Green chemistry;	A 70% B n/a C n/a
With potassium carbonate under 0.750075 - 759.826 Torr; Heating / reflux;

...Expand

: 3115-68-2
tetrabutyl phosphonium bromide

: 100-44-7
benzyl chloride

: 616-38-6
carbonic acid dimethyl ester

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
With hydrogenchloride In diethyl ether; water; N,N-dimethyl-formamide	65%

...Expand

: 59830-60-3, 63219-70-5, 68474-26-0
N-benzyloxycarbonyl-2-amino-3-phenylpropionaldehyde

: 116087-58-2
trimethyl ethoxyethyloxyphosphonoacetate

A: 13326-10-8
benzyl methyl carbonate

B: 5-Benzyl-3-(1-ethoxy-ethoxy)-1,5-dihydro-pyrrol-2-one

C: (Z)-4-Benzyloxycarbonylamino-2-(1-ethoxy-ethoxy)-5-phenyl-pent-2-enoic acid methyl ester

Conditions

Conditions	Yield
With lithium diisopropyl amide 1.) THF, -40 deg C 2.) - 40 to 25 deg C, 2 h; Yield given. Multistep reaction. Yields of byproduct given;
With lithium diisopropyl amide 1.) THF, - 40 deg C 2.) - 40 to 25 deg C, 2 h.; Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: dibutyl isocyanato methoxy tin(IV)

: 100-51-6
benzyl alcohol

A: 621-84-1
O-benzyl carbamate

B: 3459-92-5
DBC

C: 13326-10-8
benzyl methyl carbonate

D: 34833-30-2
dibutyl-bis(benzyloxy)tin

Conditions

Conditions	Yield
at 175℃; for 6h; Product distribution;

...Expand

: 3426-71-9
Benzyl N-hydroxycarbamate

: 67-56-1
methanol

: 886-65-7, 82598-07-0
1,4-diphenyl-1,3-butadiene

: benzyl 3,6-diphenyl-3,6-dihydro-2H-1,2-oxazine-2-carboxylate

B: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
With 2-ethyl-4,5-dihydrooxazole; oxygen; copper dichloride at 20℃; for 18h; Air atmosphere; chemoselective reaction;

...Expand

: C15H17NO5S

A: BrH*C7H11BrN4O

B: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: lithium azide; water / N,N-dimethyl-formamide / 2.5 h / 130 °C / Inert atmosphere 2: bromine / 0 h / 12 °C / Inert atmosphere; Darkness View Scheme

: 616-38-6
carbonic acid dimethyl ester

: 100-51-6
benzyl alcohol

: 108-93-0
cyclohexanol

A: 13326-10-8
benzyl methyl carbonate

B: 25066-36-8
methyl cyclohexyl carbonate

Conditions

Conditions	Yield
With methyl trioctylphosphonium acetate at 90℃; for 4h;

...Expand

: 124-38-9
carbon dioxide

: 100-51-6
benzyl alcohol

: 74-88-4
methyl iodide

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
Stage #1: benzyl alcohol With 1-butyl-2,3-methylimidazolium tetrafluoroborate Inert atmosphere; Electrochemical reaction; Stage #2: carbon dioxide at 40℃; under 760.051 Torr; for 2h; Stage #3: methyl iodide With potassium carbonate at 60℃; for 5h;

...Expand

: 140-11-4
Benzyl acetate

: 13326-10-8
benzyl methyl carbonate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: methanol / 2 h / 84 °C / Inert atmosphere; Schlenk technique 2: heterogeneous zinc/imidazole catalyst / 0.5 h / 100 °C / Inert atmosphere; Schlenk technique View Scheme

: 67-56-1
methanol

: 201230-82-2
carbon monoxide

: 616-38-6
carbonic acid dimethyl ester

: 100-51-6
benzyl alcohol

A: 13326-10-8
benzyl methyl carbonate

B: 101-41-7
benzeneacetic acid methyl ester

Conditions

Conditions	Yield
With palladium(II) trifluoroacetate; 1,3-bis-(diphenylphosphino)propane; caesium carbonate at 120℃; under 30003 Torr; for 24h; Reagent/catalyst;	A n/a B 47 %Chromat.

...Expand

: 1719-19-3
2-Methyl-4-phenyl-3-butyn-2-ol

: 13326-10-8
benzyl methyl carbonate

: 4980-70-5
1,3-diphenyl-1-propyne

Conditions

Conditions	Yield
With palladium diacetate; potassium carbonate; 1,4-di(diphenylphosphino)-butane In 1,4-dioxane at 120℃; for 12h; Catalytic behavior; Reagent/catalyst;	99%

: 13326-10-8
benzyl methyl carbonate

: 40888-14-0
2-methyl-4-(2-methylphenyl)-3-butyn-2-ol

: 1-methyl-2-(3-phenylprop-1-yn-1-yl)benzene

Conditions

Conditions	Yield
With palladium diacetate; potassium carbonate; 1,4-di(diphenylphosphino)-butane In 1,4-dioxane at 120℃; for 12h;	99%

: 155906-12-0
3-methyl-1-(4'-butylphenyl)-1-butyne-3-ol

: 13326-10-8
benzyl methyl carbonate

: 1-butyl-4-(3-phenylprop-1-yn-1-yl)benzene

Conditions

Conditions	Yield
With palladium diacetate; potassium carbonate; 1,4-di(diphenylphosphino)-butane In 1,4-dioxane at 120℃; for 12h;	99%

: 13326-10-8
benzyl methyl carbonate

: 83-13-6
diethyl 2-phenylmalonate

: 613670-59-0
diethyl 2-benzyl-2-phenylmalonate

Conditions

Conditions	Yield
With 1,1'-bis(diisopropylphosphino)ferrocene; {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; caesium carbonate In N,N-dimethyl-formamide at 30℃; for 48h; Inert atmosphere;	98%
With 1,1'-bis-(diphenylphosphino)ferrocene; N,O-bis-(trimethylsilyl)-acetamide; {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; potassium acetate In tetrahydrofuran at 80℃; for 24h;	95%
With 1,1'-bis-(diphenylphosphino)ferrocene; 1,5-cis,cis-cyclooctadiene; [PdCp(η3-C3H5)] In tetrahydrofuran at 80℃;	84%

: 13326-10-8
benzyl methyl carbonate

: 191162-39-7
quinolin-3-ylboronic acid

: 37045-16-2
3-benzylquinoline

Conditions

Conditions	Yield
With potassium carbonate; bis(η3-allyl-μ-chloropalladium(II)); 1,5-bis-(diphenylphosphino)pentane In N,N-dimethyl-formamide at 80℃; for 45h; Suzuki coupling;	96%

: 13326-10-8
benzyl methyl carbonate

: 150-76-5
4-methoxy-phenol

: 6630-18-8
4-methoxyphenyl benzyl ether

Conditions

Conditions	Yield
With allyl(cyclopentadiene)palladium(II); bis[2-(diphenylphosphino)phenyl] ether In toluene at 60℃; for 20.0833h; Inert atmosphere;	96%

: 13326-10-8
benzyl methyl carbonate

: 99-76-3
methyl 4-hydroxylbenzoate

: 32122-11-5
4-benzyloxy-benzoic acid methyl ester

Conditions

Conditions	Yield
With allyl(cyclopentadiene)palladium(II); bis[2-(diphenylphosphino)phenyl] ether In toluene at 60℃; for 22.0833h; Inert atmosphere;	96%

: 13326-10-8
benzyl methyl carbonate

: 108-95-2
phenol

: 946-80-5
(benzyloxy)benzene

Conditions

Conditions	Yield
With allyl(cyclopentadiene)palladium(II); bis[2-(diphenylphosphino)phenyl] ether In toluene at 60℃; for 24.0833h; Inert atmosphere;	96%

: 13326-10-8
benzyl methyl carbonate

: 873-55-2
sodium benzenesulfonate

: 3112-88-7
Benzyl phenyl sulfone

Conditions

Conditions	Yield
With bis[2-(diphenylphosphino)phenyl] ether; bis(η3-allyl-μ-chloropalladium(II)) In dimethyl sulfoxide at 80℃; for 1h;	95%

: 150-19-6
O-methylresorcine

: 13326-10-8
benzyl methyl carbonate

: 21144-16-1
3-benzyloxyanisole

Conditions

Conditions	Yield
With allyl(cyclopentadiene)palladium(II); bis[2-(diphenylphosphino)phenyl] ether In toluene at 60℃; for 24.0833h; Inert atmosphere;	94%

: 120-72-9
indole

: 13326-10-8
benzyl methyl carbonate

: 16886-11-6
3,3-dibenzyl-3H-indole

Conditions

Conditions	Yield
Stage #1: indole With {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; bis[2-(diphenylphosphino)phenyl] ether In toluene at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: benzyl methyl carbonate With N,O-bis-(trimethylsilyl)-acetamide; triethyl borane In hexane; toluene at 50℃; for 18h; Inert atmosphere;	94%

: 13326-10-8
benzyl methyl carbonate

: 1692-25-7
3-pyridylboronic acid

: 620-95-1
3-benzylpyridine

Conditions

Conditions	Yield
With potassium carbonate; bis(η3-allyl-μ-chloropalladium(II)); 1,5-bis-(diphenylphosphino)pentane In N,N-dimethyl-formamide at 80℃; for 24h; Suzuki coupling;	93%

: 13326-10-8
benzyl methyl carbonate

: 86658-78-8
N-tosyl tryptamine

: 3a-benzyl-1-tosyl-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole

Conditions

Conditions	Yield
Stage #1: N-tosyl tryptamine With {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; bis[2-(diphenylphosphino)phenyl] ether In toluene at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: benzyl methyl carbonate With N,O-bis-(trimethylsilyl)-acetamide; triethyl borane In hexane; toluene at 50℃; for 18h; Inert atmosphere;	92%

: 13326-10-8
benzyl methyl carbonate

: 79756-91-5
2-methyl-4-(4-methylphenyl)-3-butyn-2-ol

: 1-methyl-4-(3-phenylprop-1-yn-1-yl)benzene

Conditions

Conditions	Yield
With palladium diacetate; potassium carbonate; 1,4-di(diphenylphosphino)-butane In 1,4-dioxane at 120℃; for 12h;	92%

: 13331-23-2
fur-2-ylboronic acid

: 13326-10-8
benzyl methyl carbonate

: 37542-92-0
2-benzylfuran

Conditions

Conditions	Yield
With potassium carbonate; bis(η3-allyl-μ-chloropalladium(II)); 1,5-bis-(diphenylphosphino)pentane In tert-Amyl alcohol at 100℃; for 24h; Suzuki coupling;	91%

: 828-94-4
2,3-dimethyl-5-methoxyindole

: 13326-10-8
benzyl methyl carbonate

: 1350845-72-5
3-benzyl-5-methoxy-2,3-dimethyl-3H-indole

Conditions

Conditions	Yield
Stage #1: 2,3-dimethyl-5-methoxyindole With {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; bis[2-(diphenylphosphino)phenyl] ether In toluene at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: benzyl methyl carbonate With N,O-bis-(trimethylsilyl)-acetamide; triethyl borane In hexane; toluene at 50℃; for 18h; Inert atmosphere;	91%

: 13326-10-8
benzyl methyl carbonate

: 4559-70-0
Diphenylphosphine oxide

: 2959-74-2
benzyldiphenylphosphine oxide

Conditions

Conditions	Yield
With bis(η3-allyl-μ-chloropalladium(II)); bis[2-(diphenylphosphino)phenyl] ether In N,N-dimethyl-formamide at 100℃; for 48h; Inert atmosphere; Sealed tube;	91%

: 13326-10-8
benzyl methyl carbonate

: 5720-07-0
4-methoxyphenylboronic acid

: 834-14-0
p-benzylanizole

Conditions

Conditions	Yield
With 1,5-bis-(diphenylphosphino)pentane; potassium carbonate; bis(η3-allyl-μ-chloropalladium(II)) In N,N-dimethyl-formamide at 80℃; for 24h; Suzuki-Miyaura reaction;	90%

: 13326-10-8
benzyl methyl carbonate

: 106-48-9
4-chloro-phenol

: 7700-27-8
4-chlorophenyl benzyl ether

Conditions

Conditions	Yield
With allyl(cyclopentadiene)palladium(II); bis[2-(diphenylphosphino)phenyl] ether In toluene at 60℃; for 16.0833h; Inert atmosphere;	90%

: 942-01-8
1,2,3,4-tetrahydrocarbazole

: 13326-10-8
benzyl methyl carbonate

: 18781-55-0
4a-benzyl-2,3,4,4a-tetrahydro-1H-carbazole

Conditions

Conditions	Yield
Stage #1: 1,2,3,4-tetrahydrocarbazole With {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; bis[2-(diphenylphosphino)phenyl] ether In toluene at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: benzyl methyl carbonate With N,O-bis-(trimethylsilyl)-acetamide; triethyl borane In hexane; toluene at 50℃; for 18h; Inert atmosphere;	90%

: 13326-10-8
benzyl methyl carbonate

: 1068-90-2
2-acetylaminomalonic acid diethyl ester

: 3235-26-5
2-(N-acetylamino)-2-benzylpropanedioic diethyl ester

Conditions

Conditions	Yield
With 1,1'-bis-(diphenylphosphino)ferrocene; N,O-bis-(trimethylsilyl)-acetamide; {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; potassium acetate In tetrahydrofuran at 80℃; for 48h;	89%

: 576-26-1
2.6-dimethylphenol

: 13326-10-8
benzyl methyl carbonate

: 19578-74-6
1,3-Dimethyl-2-(phenylmethoxy)benzene

Conditions

Conditions	Yield
With allyl(cyclopentadiene)palladium(II); bis[2-(diphenylphosphino)phenyl] ether In toluene at 60℃; for 3.08333h; Inert atmosphere;	89%

: 1350845-99-6
2-trityl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole

: 13326-10-8
benzyl methyl carbonate

: 1350845-91-8
4a-benzyl-2-trityl-2,3,4,4a-tetrahydro-1H-pyrido[3,4-b]indole

Conditions

Conditions	Yield
Stage #1: 2-trityl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole With {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; bis[2-(diphenylphosphino)phenyl] ether In toluene at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: benzyl methyl carbonate With N,O-bis-(trimethylsilyl)-acetamide; triethyl borane In hexane; toluene at 50℃; for 18h; Inert atmosphere;	89%

: 5018-30-4
dimethyl methoxymalonate

: 13326-10-8
benzyl methyl carbonate

: 124604-07-5
dimethyl O-methylbenzyltartronate

Conditions

Conditions	Yield
With 1,1'-bis-(diphenylphosphino)ferrocene; N,O-bis-(trimethylsilyl)-acetamide; {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; potassium acetate In tetrahydrofuran at 80℃; for 48h;	88%

: 83-34-1
3-Methylindole

: 13326-10-8
benzyl methyl carbonate

: 19013-48-0
3-benzyl-3-methyl-3H-indole

Conditions

Conditions	Yield
Stage #1: 3-Methylindole With {(η4-1,5-cyclooctadiene)Pd(η3-allyl)}BF4; bis[2-(diphenylphosphino)phenyl] ether In toluene at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: benzyl methyl carbonate With N,O-bis-(trimethylsilyl)-acetamide; triethyl borane In hexane; toluene at 50℃; for 18h; Inert atmosphere;	88%

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