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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1697718생성일: 2026년 10월 27일

Isopropyl Acetate → 5-(4-tert-Butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/1697718

반응식

참여 물질

역할이름HCID투입량
반응물Isopropyl AcetateHCID 7915—
반응물TriethylamineHCID 8471—
반응물Phenyl vinyl sulfoneHCID 79664—
반응물Lithium BromideHCID 82050—
반응물HCID 178472689HCID 178472689—
용매TetrahydrofuranHCID 8028—
생성물5-(4-tert-Butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic Acid Ethyl EsterHCID 667708288%

반응 단계

To a stirred solution of (E)-ethyl 2-(4-tert-butylbenzylideneamino)acetate (226 mg, 914 umol; example 441a) in THF (5 ml) under an argon atmosphere were added lithium bromide (119 mg, 1.37 mmol), triethylamine (191 ul, 1.37 mmol) and phenyl vinyl sulfone (154 mg, 914 umol; CAS Reg. No. 5535-48-8). The mixture was stirred at ambient temperature for 20 h. iPrOAc (50 ml) and ice water (40 ml) were added and the layers were separated. The organic layer was washed with brine (40 ml), dried over sodium sulfate and filtered. The solvent was removed under reduced pressure to give a yellow oil which was purified by column chromatography (silica gel, iPrOAc/n-heptane) to obtain the title compound (56 mg, 73 umol; 8%) as colorless solid. MS (ESI): m/z=416.2 [M+H]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163793B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-4a5887a39fce47c6962960c891c32db4
출처 메모uspto-grants-2012_04