4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
CAS No.:856660-74-7
Molecular Formula:C₄₈H₆₂N₂O₉SSi
Molecular Weight:871.18
Hs Code.:

4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(<i>tert</i>-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid <i>tert</i>-butyl ester

Synonyms:4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Suppliers and Price of 4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

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 4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

There total 12 articles about 4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 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:

: 67436-17-3
dimethyl (S)-N-(benzyloxycarbonyl)glutamate

: 856660-74-7
4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 79 percent / LiBH₄ / methanol; tetrahydrofuran / 4 h / 0 °C

2: 88 percent / pTsOH / CH₂Cl₂ / 24 h / 20 °C

3: 27.4 g / Et₃N / CH₂Cl₂ / 0.5 h / -20 °C

4: tetrahydrofuran / 1 h / 0 - 20 °C

5: 31.4 g / magnesium monoperoxy phthalate / ethanol / 0 °C

6: 24.1 g / CeCl₃*7H₂O; (COOH)2 / acetonitrile / 20 °C

7: 38.6 g / imidazole / dimethylformamide / 2 h / 20 °C

8: 85 percent / nBuLi / tetrahydrofuran; hexane / 2.33 h / -78 - 20 °C

9: 95 percent / o-iodoxybenzoic acid / dimethylsulfoxide / 4 h / 20 °C

With 1H-imidazole; lithium borohydride; n-butyllithium; cerium(III) chloride; oxalic acid; toluene-4-sulfonic acid; magnesium monoperoxyphthalate hexahydrate; triethylamine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/ejoc.200400709

Reference yield:

: 13574-13-5
Boc-Glu(OBzl)-OH

: 856660-74-7
4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: N-hydroxysuccinimide; DCC / ethyl acetate / 20 °C

1.2: 81 percent / NaBH₄ / ethanol; tetrahydrofuran / 0.5 h / 0 °C

2.1: 92 percent / pTsOH / 48 h / 20 °C

3.1: 96 percent / LiAlH₄ / tetrahydrofuran / 0.25 h / 0 °C

4.1: 98 percent / DMSO; oxalyl chloride; Et₃N / CH₂Cl₂ / 2 h / -78 - 20 °C

5.1: 85 percent / nBuLi / tetrahydrofuran; hexane / 2.33 h / -78 - 20 °C

6.1: 95 percent / o-iodoxybenzoic acid / dimethylsulfoxide / 4 h / 20 °C

With 1-hydroxy-pyrrolidine-2,5-dione; lithium aluminium tetrahydride; n-butyllithium; oxalyl dichloride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; dicyclohexyl-carbodiimide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; hexane; dichloromethane; dimethyl sulfoxide; ethyl acetate; 4.1: Swern oxidation;
DOI:10.1002/ejoc.200400709

Reference yield:

: 144090-56-2
2,2-dimethyl-3-<(1,1-dimethylethoxy)carbonyl>-4(S)-oxazolidinepropanal

: 856660-74-7
4-[4-benzenesulfonyl-7-benzyloxycarbonylamino-8-(tert-butyl-diphenyl-silanyloxy)-3-oxo-octyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / nBuLi / tetrahydrofuran; hexane / 2.33 h / -78 - 20 °C

2: 95 percent / o-iodoxybenzoic acid / dimethylsulfoxide / 4 h / 20 °C

With n-butyllithium; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; hexane; dimethyl sulfoxide;
DOI:10.1002/ejoc.200400709