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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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물(2S,4S)-1-((Benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688414—
반응물1,1-Difluoro-2-(trifluoromethylsulfonyl)ethaneHCID 86643803—
용매TetrahydrofuranHCID 8028—
생성물(2S,4S)-1-(Benzyloxycarbonyl)-4-(2,2-difluoroethoxy)pyrrolidine-2-carboxylic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08415340B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-0164ecd3a2e74145a500b8a25cf26140
출처 메모uspto-grants-2013_04