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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339706생성일: 2026년 10월 24일

Trifluoroacetic acid → benzyl N-[(3R,4S)-3-fluoropiperidin-4-yl]carbamate

https://huagongshe.com/ko/reaction/339706

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물HCID 86708534HCID 86708534—
용매DichloromethaneHCID 6344—
생성물benzyl N-[(3R,4S)-3-fluoropiperidin-4-yl]carbamateHCID 6856655479.2%

반응 단계

(cis)-tert-Butyl 4-(benzyloxycarbonylamino)-3-fluoropiperidine-1-carboxylate (7.5 g, 21.3 mmol) was weighed into a 500 mL 1 neck round bottom and dissolved in 200 mL of DCM, followed by addition of TFA (16.4 mL, 213 mmol) and stirring at ambient temperature for 1 hour, at which time all bubbling had ceased and the reaction appeared complete by TLC. The crude reaction was concentrated in vacuo, followed by aqueous work-up with 2 N NaOH and DCM. The combined organics were dried over Na2SO4, filtered and concentrated in vacuo to afford benzyl(cis)-3-fluoropiperidin-4-ylcarbamate (4.25 g, 16.8 mmol, 79.2% yield) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895550B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-98909412d28e4f92a1b3ae15ba9a7b97
출처 메모uspto-grants-2014_11