tert-butyl 2-methylene-3-oxo-1-(3-(trifluoromethyl)phenyl)butyl carbonate

Base Information

Chemical Name:tert-butyl 2-methylene-3-oxo-1-(3-(trifluoromethyl)phenyl)butyl carbonate
CAS No.:1308286-07-8
Molecular Formula:C₁₇H₁₉F₃O₄
Molecular Weight:344.331
Hs Code.:

Synonyms:tert-butyl 2-methylene-3-oxo-1-(3-(trifluoromethyl)phenyl)butyl carbonate

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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 tert-butyl 2-methylene-3-oxo-1-(3-(trifluoromethyl)phenyl)butyl carbonate

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Technology Process of tert-butyl 2-methylene-3-oxo-1-(3-(trifluoromethyl)phenyl)butyl carbonate

There total 1 articles about tert-butyl 2-methylene-3-oxo-1-(3-(trifluoromethyl)phenyl)butyl carbonate 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: 61.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 1308286-10-3
C₁₂H₁₁F₃O₂

: 1308286-07-8
tert-butyl 2-methylene-3-oxo-1-(3-(trifluoromethyl)phenyl)butyl carbonate

Guidance literature:: With dmap; In dichloromethane; at 20 ℃;
DOI:10.1039/c1ob00017a

Reference yield:

: 28897-81-6,51127-17-4,85700-33-0,5839-93-0
2-phenyl-4-iso-propyl-4H-oxazolin-5-one

: 1308286-07-8
tert-butyl 2-methylene-3-oxo-1-(3-(trifluoromethyl)phenyl)butyl carbonate

: 1308285-87-1
(S)-4-isorpopyl-4-((R)-2-methylene-3-oxo-1-(3-(trifluorophenyl))butyl)-2-phenyloxazol-5(4H)-one

: 4-isorpopyl-4-(2-methylene-3-oxo-1-(3-(trifluorophenyl))butyl)-2-phenyloxazol-5(4H)-one

Guidance literature:: With (R)-1-benzyl-3-(2'-(bis(3,5-dimethylphenyl)phosphino)-1,1'-binaphthyl-2-yl)thiourea; In dichloromethane; at 20 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1039/c1ob00017a