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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 565679생성일: 2026년 10월 23일

Trifluoroacetic acid → 1-Phenyl-3-(1,2,3,6-tetrahydro-4-pyridyl)-1H-indole

https://huagongshe.com/ko/reaction/565679

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물1-Phenyl-1H-indoleHCID 182029—
반응물PiperonylamineHCID 2723901—
반응물Azane;hydrateHCID 12896473—
용매Acetic AcidHCID 176—
생성물1-Phenyl-3-(1,2,3,6-tetrahydro-4-pyridyl)-1H-indoleHCID 2211112763%

반응 조건

온도120 °C

반응 단계

To a heated (110° C.) mixture of 4-piperidone monohydrate hydrochloride (8.2 g), acetic acid (15 mL) and trifluoroacetic acid (30 mL) was added 1-phenyl-1H-indole (3.1 g) under nitrogen atmosphere over a period of 25 min. The mixture was stirred for 30 minutes at 120° C., then cooled and poured into ice. This was neutralized with conc. ammonia water under cooling and the product was extracted thrice with ethyl acetate. The combined extract was washed with water followed by saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was provided for the next reaction without further purification. Yield 63%. Amorphous.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06172085B2
출처 데이터셋uspto-grants-2001_01
ORD IDord-962fd7bdf84944b1a7453bfae665d5d4
출처 메모uspto-grants-2001_01