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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1180115생성일: 2026년 10월 27일

Sodium Fluoride → (2S,4S)-1-Benzyl 2-methyl 4-fluoropyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1180115

반응식

참여 물질

역할이름HCID투입량
반응물Sodium FluorideHCID 5235—
반응물2-Methyl 1-(phenylmethyl) (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylateHCID 688411—
반응물HCID 131726637HCID 131726637—
용매DichloromethaneHCID 6344—
생성물(2S,4S)-1-Benzyl 2-methyl 4-fluoropyrrolidine-1,2-dicarboxylateHCID 1163772274.7%

반응 단계

Methyl(2S,4R)-1-benzyloxycarbonyl-4-hydroxypyrrolidine-2-carboxylate (306 mg, 0.00108 mol) and sodium fluoride (55 mg, 0.00131 mol) were suspended in dichloromethane (1.8 mL), followed by addition of Ishikawa reagent (293 mg, 0.00131 mol) under ice cooling. The reaction mixture was slowly warmed to room temperature and then stirred for 20 hours. After the reaction, the reaction mixture was poured into ice-cold saturated aqueous sodium bicarbonate (5 mL) and then separated into organic and aqueous layers. The aqueous layer was extracted with ethyl acetate. This extracted solution was combined with the organic layer obtained above, washed sequentially with 10% aqueous potassium bisulfate and saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate. After drying, the solvent and the decomposition product of Ishikawa reagent (N,N-diethyl-2,3,3,3-tetrafluoropropionamide) were distilled off under reduced pressure, and the residue was applied to silica gel column chromatography (developing solvent; hexane:ethyl acetate=5:1 to 0:1) to give the titled compound (227 mg, colorless oil).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07279584B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-20047f658506466f89d50a259df1cdfb
출처 메모uspto-grants-2007_10