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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43339생성일: 2026년 10월 23일

Acetic Acid → tert-Butyl 4-(3-fluoroanilino)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/43339

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3-FluoroanilineHCID 9742—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 4-(3-fluoroanilino)piperidine-1-carboxylateHCID 2313759182%

반응 단계

A solution of 1,1-dimethylethyl 4-oxo-1-piperidinecarboxylate (1.91 g, 9.53 mmol), 3-fluoroaniline (1.06, 9.53 mmol) and acetic acid (0.55 ml, 9.53 mmol) in 1,2-DCE (50 ml) was stirred at room temperature overnight. Sodium tri(acetoxy)borohydride (2.82 g, 13.3 mmol) was then added, stirred for 8 hrs and then allowed to stand at room temperature. The reaction mixture was diluted with DCM and washed with NaHCO3 solution, dried over MgSO4 and then concentrated to give the product which was purified by column chromatography. Elution with 0-40% EtOAc/pentane gave the title compound as a white solid (2.3 g). δH (CDCl3, 250 MHz) 7.08 (1H, q), 6.35 (3H, m), 4.04 (1H, br s), 3.65 (1H, br s), 3.38 (1H, m), 2.92 (2H, m), 2.02 (2H, m), 1.47 (9H, s), 1.34 (2H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536182B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ed5e4844a6594da5b9d1c7dabd6a94e7
출처 메모uspto-grants-2013_09