(R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate

Base Information

Chemical Name:(R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate
CAS No.:1174013-25-2
Molecular Formula:C₁₀H₁₅F₃O₅S
Molecular Weight:304.287
Hs Code.:

Synonyms:(R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate

Suppliers and Price of (R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate

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

Crysdot
(R)-Methyl3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)propanoate 97%
1g
$ 434.00

Total 2 raw suppliers

Chemical Property of (R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate

Chemical Property:

Purity/Quality:

97% ^*data from raw suppliers

(R)-Methyl3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)propanoate 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate

There total 3 articles about (R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate 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: 96.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 1174013-24-1
(R)-methyl 3-cyclopentyl-2-hydroxypropanoate

: 1174013-25-2
(R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1016/j.bmcl.2009.04.107

Reference yield:

: 33240-34-5
cyclopentylmagnesium bromide

: 1174013-25-2
(R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: dilithium tetrachlorocuprate / tetrahydrofuran; diethyl ether / 0.5 h / -50 - -10 °C

1.2: 0.83 h / -78 - -50 °C

1.3: 0.5 h

2.1: 2,6-dimethylpyridine / dichloromethane / 0.75 h / 0 °C / Inert atmosphere

With 2,6-dimethylpyridine; dilithium tetrachlorocuprate; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/jm2014887

Reference yield:

: 1401513-92-5
C₉H₁₄O₃

: 1174013-25-2
(R)-methyl 3-cyclopentyl-2-(((trifluoromethyl)sulfonyl)oxy)-propanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: alcohol dehydrogenase T / isopropyl alcohol / 35 °C / pH 6.5 - 7.5

2.1: 2,6-dimethylpyridine / hexane; toluene / 2.5 h / -15 - 0 °C

2.2: 0.83 h / 10 - 20 °C

With 2,6-dimethylpyridine; In hexane; isopropyl alcohol; toluene;
DOI:10.1021/op300194c