benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate

Base Information

Chemical Name:benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate
CAS No.:1647153-71-6
Molecular Formula:C₂₁H₃₁NO₅
Molecular Weight:377.481
Hs Code.:

Synonyms:benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate

Suppliers and Price of benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate

There total 5 articles about benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 82.0%

: 1449475-66-4
(4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylic acid

: 100-39-0
benzyl bromide

: 1647153-71-6
benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 20h; Inert atmosphere;
DOI:10.3762/bjoc.10.113

Reference yield:

: 1647153-47-6
(2R,3S)-2-(tert-butyloxycarbonylamino)-1-O-(tert-butyldimethylsilyl)-4-methyl-pentane-1,3-diol

: 1647153-71-6
benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: boron trifluoride diethyl etherate / acetone / 23 h / 20 °C

2: ruthenium trichloride; sodium periodate / water; tetrachloromethane; acetonitrile / 4 h / 0 °C

3: caesium carbonate / N,N-dimethyl-formamide / 20 h / 20 °C / Inert atmosphere

With ruthenium trichloride; sodium periodate; boron trifluoride diethyl etherate; caesium carbonate; In tetrachloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.3762/bjoc.10.113

Reference yield:

: 188802-09-7
(2R,3S)-1-(tert-Butyl-dimethyl-silanyloxy)-2-dibenzylamino-4-methyl-pentan-3-ol

: 1647153-71-6
benzyl (4S,5S)-N-(tert-butyloxycarbonyl)-5-isopropyl-2,2-dimethyloxazolidine-4-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: 10 wt% Pd(OH)2 on carbon; hydrogen / methanol

2: sodium hydrogencarbonate / tetrahydrofuran; water / 19 h / 0 - 20 °C

3: boron trifluoride diethyl etherate / acetone / 23 h / 20 °C

4: ruthenium trichloride; sodium periodate / water; tetrachloromethane; acetonitrile / 4 h / 0 °C

5: caesium carbonate / N,N-dimethyl-formamide / 20 h / 20 °C / Inert atmosphere

With ruthenium trichloride; sodium periodate; 10 wt% Pd(OH)2 on carbon; boron trifluoride diethyl etherate; hydrogen; sodium hydrogencarbonate; caesium carbonate; In tetrahydrofuran; methanol; tetrachloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.3762/bjoc.10.113