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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536587생성일: 2026년 10월 25일

4-Nitrobenzoic Acid → HCID 66848190, 화합물

https://huagongshe.com/reaction/536587

반응식

참여 물질

역할이름HCID투입량
반응물4-Nitrobenzoic AcidHCID 6108—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물tert-butyl (2S,4R)-4-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 11078078—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물HCID 66848190HCID 66848190—

반응 조건

온도0 °C

반응 단계

(2S,4R)-4-(Tert-butyl-dimethyl-silanyloxy)-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (intermediate 53, 51.4 g, 155 mmol) dissolved in 500 ml of dichloromethane was cooled to 0° C., then p-nitrobenzoic acid (28.5 g, 171 mmol), N,N′-dicyclohexylcarbodiimide (35.2 g, 171 mmol) and 4-dimethylaminopyridine (1.90 g, 1.60 mmol) were added. The mixture was maintained under stirring at room temperature for 18 hours, then filtrated; the filtrate was concentrated to obtain crude that was purified by silica gel chromatography (petroleum ether/ethyl acetate from 15/1 to 10/1). (2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(4-nitro-benzoyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester was obtained as white solid (70 g, yield: 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859608B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-aedafc3454554af78953524a7ae56442
출처 메모uspto-grants-2014_10