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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 591346생성일: 2026년 10월 26일

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/reaction/591346

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Trifluoroacetic acidHCID 6422—
반응물HexaneHCID 8058—
반응물Tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylateHCID 89613009—
용매DichloromethaneHCID 6344—
생성물Hydrochloric AcidHCID 313—
생성물6-Fluoro-1-(piperidin-4-yl)indolineHCID 22038384—

반응 단계

To a solution of tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylate (16.64 g, 52 mmol) in CH2Cl2 (45 mL) was added TFA (30 mL) slowly at room temperature. The resulting mixture was stirred at room temperature for 3 h. The resulting mixture was concentrated to remove most of solvent and TFA. The resulting residue was partitioned in CH2Cl2/H2O (100 mL/50 mL) and stirred. 3N NaOH(aq) was added slowly until the pH value of aqueous layer was >11. The aqueous layer was then extracted with CH2Cl2 (100 mL×10). The combined CH2Cl2 layer was dried (Na2SO4) and filtered. The solvent was removed by roto-evaporator, the resulting residue was dissolved in Et2O (100 mL) and 1N HCl (1M in Et2O, 60 mL, 60 mmol) was added slowly at 0° C. Then, the resulting mixture was allowed to warm to room temperature for another 30 min. Hexane (100 mL) was added and stirred for 15 min. The resulting white solid was filtered and washed with 50% Et2O/hexane (30 mL×3), then dried to yield 6-fluoro-1-(piperidin-4-yl)indoline as a white HCl salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09238658B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-190dc9512be14a81b03f30338c7d34ce
출처 메모uspto-grants-2016_01