Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1961416생성일: 2026년 10월 27일
Sodium hydride → (2S,4S)-1-(Benzyloxycarbonyl)-4-(2,2-difluoroethoxy)pyrrolidine-2-carboxylic acid
https://huagongshe.com/reaction/1961416
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | (2S,4S)-1-((Benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acid | HCID 688414 | — |
| 반응물 | 1,1-Difluoro-2-(trifluoromethylsulfonyl)ethane | HCID 86643803 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2S,4S)-1-(Benzyloxycarbonyl)-4-(2,2-difluoroethoxy)pyrrolidine-2-carboxylic acid | HCID 59436454 | — |
반응 단계
To a solution of (2S,4S)-1-(benzyloxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid (5.0 g, 18.85 mmol) in THF (100 mL) was added NaH (1.583 g, 39.6 mmol) at 0° C. under N2. The resulting suspension was stirred at RT for 30 min. A solution of 1,1-difluoro-2-(trifluoromethylsulfonyl)ethane (4.11 g, 20.73 mmol) in THF (5 ml) was added to the suspension. The reaction mixture was stirred at RT for 3 h. The reaction mixture was quenched with water and concentrated. The residue was extracted with EtOAc; the aqueous layers was acidified to ph 3 with 1N HCl and extracted with EtOAc. The organic layers were washed with water and brine, dried over Na2SO4, and filtered. The crude product was used in the next step without purification. LC/MS [M−H]+: 328; Ret time (Method F): 0.93 min (Phenomenex-Luna s10 4.6×50 mm column, 4 min gradient, 4 mL/min).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08415340B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-0164ecd3a2e74145a500b8a25cf26140 |
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| 출처 메모 | uspto-grants-2013_04 |
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