돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 553922생성일: 2026년 10월 26일

Water → ethyl (R)-2-tert-butoxycarbonylamino-5-(3,4-difluorophenyl)-5-oxovalerate

https://huagongshe.com/reaction/553922

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Boc-D-Pyroglutamic acid ethyl esterHCID 820885—
반응물HCID 178505835HCID 178505835—
용매TetrahydrofuranHCID 8028—
생성물ethyl (R)-2-tert-butoxycarbonylamino-5-(3,4-difluorophenyl)-5-oxovalerateHCID 67373437—

반응 단계

To a solution of (R)-5-oxopyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (6.0 g) in tetrahydrofuran (100 mL), 3,4-difluorophenylmagnesium bromide (0.5 M solution in tetrahydrofuran; 50 mL) was added dropwise at −40° C. over 10 minutes, and the reaction solution was stirred at −40° C. to 0° C. for two hours. Water was added to the solution in small portions, followed by extraction with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate system) to obtain 8.3 g of the title compound. The property values of the compound are as follows.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048878B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-848be85c996c41afa02ae8fcda00e084
출처 메모uspto-grants-2011_11