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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isopropyl Acetate | HCID 7915 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Phenyl vinyl sulfone | HCID 79664 | — |
| 반응물 | Lithium Bromide | HCID 82050 | — |
| 반응물 | HCID 178472689 | HCID 178472689 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-(4-tert-Butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic Acid Ethyl Ester | HCID 66770828 | 8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08163793B2 |
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| 출처 데이터셋 | uspto-grants-2012_04 |
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| ORD ID | ord-4a5887a39fce47c6962960c891c32db4 |
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| 출처 메모 | uspto-grants-2012_04 |
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