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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1348593생성일: 2026년 10월 25일

Sodium hydride → (S)-2-tert-Butoxycarbonylamino-3-(2-methyl-6-nitro-phenoxy)-propionic acid benzyl ester

https://huagongshe.com/reaction/1348593

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Methyl-6-nitrophenolHCID 83103—
반응물4-Benzyl 3-(tert-butyl) (S)-1,2,3-oxathiazolidine-3,4-dicarboxylate 2,2-dioxideHCID 86605284—
용매DimethylformamideHCID 6228—
생성물(S)-2-tert-Butoxycarbonylamino-3-(2-methyl-6-nitro-phenoxy)-propionic acid benzyl esterHCID 6707673733%

반응 단계

In an inert atmosphere and under exclusion of moisture, at 0° C. a solution of 1.5 g (10 mmol) of 2-methyl-6-nitro-phenol [Ger.Offen. 3536192] in 30 ml of N,N-dimethylformamide was treated portionwise with 0.42 g (18 mmol) of sodium hydride (55% dispersion in mineral oil). After complete addition, stirring was continued for 1 hour at 0° C. Thereafter, 3.85 g (11 mmol) of (S)-2,2-dioxo-2λ6-[1,2,3]oxathiazolidine-3,4-dicarboxylic acid 4-benzyl ester 3-tert-butyl ester was added and stirring continued at 0° C. for 3 hours, then at room temperature overnight. For the working-up, the solvent was evaporated under reduced pressure, the residue treated with 100 ml of hydrochloric acid (1 N), then extracted 3 times with 150 ml of ethyl acetate. The crude product (4.0 g) was obtained as a dark brown oil which was purified by flash-chromatography on silica gel using a gradient of a 100%:0%- to 50%:50%-mixture of heptane and ethyl acetate as the eluent. There were obtained 1.4 g (33%) of the title compound as an yellow oil, [α]589=−1.45° (c=1.0% in MeOH), MS m/e (%): 431.4 (M+H+, 13).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07211573B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-53a20fc3df5941e8ba2bc65252e79304
출처 메모uspto-grants-2007_05