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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1242543생성일: 2026년 10월 25일

Pyridine → (2S,4EZ)-4-[(allyloxy)imino)-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxylic acid

https://huagongshe.com/reaction/1242543

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물(2S)-1-(tert-butoxycarbonyl)-4-oxopyrrolidine-2-carboxylic acidHCID 11593804—
반응물O-Prop-2-en-1-ylhydroxylamine--hydrogen chloride--water (1/1/1)HCID 16211718—
용매EthanolHCID 702—
생성물(2S,4EZ)-4-[(allyloxy)imino)-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxylic acidHCID 5871456294.3%

반응 단계

A solution was made containing (2S)-1-(tert-butoxycarbonyl)-4-oxo-2-pyrrolidinecarboxylic acid (Intermediate 1, 5.0 g, 22 mmol) and O-allylhydroxylamine hydrochloride monohydrate (7.2 g, 65.5 mmol) in a 1:1 mixture of pyridine and ethanol (100 ml). The reaction was heated to reflux for 2.5 h before cooling and removal of solvent. The residue was dissolved in ethyl acetate and washed rapidly with 1.3N HCl (40 ml). The acidic layer was then extracted with ethyl acetate (3×20 ml) and the combined organic layers washed with brine before drying over magnesium sulfate, filtering and removal of solvent in vacuo. The desired product (5.9 g, 94%) was isolated as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07115639B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-e25bdd105f094a92a2614a2391678a3d
출처 메모uspto-grants-2006_10