(S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Base Information

Chemical Name:(S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
CAS No.:1364681-46-8
Molecular Formula:C₃₁H₃₆F₃NO₆
Molecular Weight:575.625
Hs Code.:

Synonyms:(S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Suppliers and Price of (S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

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 (S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

There total 6 articles about (S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate 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: 86.0%

: 1364680-62-5
(S)-4-benzyl-3-((4R,5R,E)-5-hydroxy-2,4,7-trimethyloct-2-enoyl)oxazolidin-2-one

: 20445-33-4,39637-99-5
(R)-methoxytrifluoromethylphenylacetyl chloride

: 1364681-46-8
(S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 16h;
DOI:10.1021/ol300353w

Reference yield:

: 15790-87-1,818-59-7,15790-88-2
Methyl (E)-2-pentenoate

: 1364681-46-8
(S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; lithium diisopropyl amide / tetrahydrofuran; hexane / 1 h / -78 °C / Inert atmosphere

1.2: 0.33 h / -78 °C / Inert atmosphere

2.1: water; lithium hydroxide / methanol; diethyl ether / 5 h / 20 °C

3.1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 16 h / 0 - 20 °C

4.1: sodium hexamethyldisilazane / tetrahydrofuran / 1.5 h / -78 °C / Inert atmosphere

4.2: 1.25 h / -78 °C / Inert atmosphere

5.1: titanium tetrachloride / dichloromethane / 0.17 h / -78 °C / Inert atmosphere

5.2: 16 h / -78 °C / Inert atmosphere

6.1: dmap; triethylamine / dichloromethane / 16 h / 20 °C

With dmap; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; water; sodium hexamethyldisilazane; titanium tetrachloride; triethylamine; dicyclohexyl-carbodiimide; lithium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; 5.2: Kobayashi aldol reaction;
DOI:10.1021/ol300353w

Reference yield:

: 1364680-56-7
(S)-4-benzyl-3-((1E,3Z)-1-((tert-butyldimethylsilyl)oxy)-2-methylpenta-1,3-dien-1-yl)oxazolidin-2-one

: 1364681-46-8
(S)-(4R,5R,E)-8-((S)-4-benzyl-2-oxooxazolidin-3-yl)-2,5,7-trimethyl-8-oxooct-6-en-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: titanium tetrachloride / dichloromethane / 0.17 h / -78 °C / Inert atmosphere

1.2: 16 h / -78 °C / Inert atmosphere

2.1: dmap; triethylamine / dichloromethane / 16 h / 20 °C

With dmap; titanium tetrachloride; triethylamine; In dichloromethane; 1.2: Kobayashi aldol reaction;
DOI:10.1021/ol300353w