Benzeneacetic acid, a-hydroxy-, butyl ester, (R)-

Base Information

Chemical Name:Benzeneacetic acid, a-hydroxy-, butyl ester, (R)-
CAS No.:119656-72-3
Molecular Formula:C12H16O3
Molecular Weight:208.257
Hs Code.:

Synonyms:

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

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Chemical Property of Benzeneacetic acid, a-hydroxy-, butyl ester, (R)-

Chemical Property:

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Safty Information:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

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Technology Process of Benzeneacetic acid, a-hydroxy-, butyl ester, (R)-

There total 10 articles about Benzeneacetic acid, a-hydroxy-, butyl ester, (R)- 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: 85.0%

: 611-71-2
(R)-Mandelic Acid

: 71-36-3
butan-1-ol

: 119656-72-3,119718-90-0
(R)-mandelic acid n-butyl ester

Guidance literature:: With toluene-4-sulfonic acid; In toluene; Heating;
DOI:10.1016/S0040-4020(01)85370-9

Reference yield: 76.0%

: 5524-55-0
n-butyl 2-oxo-2-phenylacetate

: 119656-72-3,119718-90-0
(R)-mandelic acid n-butyl ester

Guidance literature:: With cyclohexanone monooxygenase mutant L₁₄₃F from Acinetobacter sp. NCIMB 9871 in Escherichia coli whole-cell culture medium; In acetonitrile; at 20 ℃; enantioselective reaction; Catalytic behavior; Inert atmosphere; Microbiological reaction; Enzymatic reaction;
DOI:10.1002/anie.201907606

Reference yield: 30.0%

: 14007-02-4,119718-90-0
butyl mandelate

: 5524-55-0
n-butyl 2-oxo-2-phenylacetate

: 119656-72-3,119718-90-0
(R)-mandelic acid n-butyl ester

Guidance literature:: With 2,2,6,6-tetramethyl-piperidine-N-oxyl; N,N’-bis(salicylidene)-1,1’-binaphthyl-2,2’-diamine; oxygen; cobalt(II) diacetate tetrahydrate; In toluene; at 90 ℃; for 8h; under 760.051 Torr; optical yield given as %ee; enantioselective reaction;
DOI:10.1039/c0cc01917h