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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1187778생성일: 2026년 10월 27일

(S)-4-[(E)-2-(6-chloro-pyridin-3-yl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester → (S)-4-[2-(6-chloro-pyridin-3-yl)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1187778

반응식

참여 물질

역할이름HCID투입량
반응물(S)-4-[(E)-2-(6-chloro-pyridin-3-yl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 86664598—
촉매PlatinumHCID 23939—
용매MethanolHCID 887—
생성물(S)-4-[2-(6-chloro-pyridin-3-yl)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 8666459794.3%

반응 단계

To a stirred suspension of (S)-4-[(E)-2-(6-chloro-pyridin-3-yl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (1.0 g) in methanol (70 ml) was added platinum on charcoal (0.58 g, 10 wt %) and the mixture was stirred under an atmosphere of hydrogen at room temperature for 15 min. The mixture was then filtered through celite and the filtrate was concentrated in vacuo to give (S)-4-[2-(6-chloro-pyridin-3-yl)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (949 mg, 94%) as a colourless oil. MS (ISP): 343.2 ([{37Cl}M+H]+), 341.1 ([{35Cl}M+H]+), 287.0 ([{37Cl}M+H—C4H8]+), 285.1 ([{35Cl}M+H—C4H8]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673950B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-e2dec380e5c843d6bdc4cc29bb60b0d4
출처 메모uspto-grants-2014_03