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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 906348생성일: 2026년 10월 24일

Trifluoroacetic acid → 4-(3-Fluorophenoxy)piperidine

https://huagongshe.com/reaction/906348

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Tert-butyl 4-(3-fluorophenoxy)piperidine-1-carboxylateHCID 57699520—
용매DichloromethaneHCID 6344—
생성물4-(3-Fluorophenoxy)piperidineHCID 18524002111.8%

반응 단계

A solution of 1,1-dimethylethyl 4-[(3-fluorophenyl)oxy]-1-piperidinecarboxylate (D11) (16.4 g, 55 mmol) in DCM (200 ml) at 0° C. was treated with TFA (17 ml). The reaction was warmed to room temperature and stirred overnight. The solvent was then removed in vacuo and the residue partitioned between DCM and 2M NaOH solution. The aqueous was further extracted with DCM (×2) and the combined organics concentrated in vacuo. The residue was re-dissolved in DCM and extracted with 2M HCl (×2) which was then basified with 2M NaOH and re-extracted with DCM (×3). The combined organics were concentrated in vacuo to give the title compound (12 g). δH (CDCl3, 250 MHz) 1.66 (2H, m), 2.01 (2H, m), 2.73 (2H, m), 3.14 (2H, m), 4.34 (1H, m), 6.68 (3H, m), 7.19 (1H, m), MS (ES): MH+ 196. This whole was diluted with MeOH and treated with 1M HCl in Et2O to give the hydrochloride salt of the title compound (8.0 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08012981B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-a2881ee2bc494afc87a53d881073b817
출처 메모uspto-grants-2011_09