돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 966973생성일: 2026년 10월 25일

Benzyl Bromide → 1-Benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine

https://huagongshe.com/reaction/966973

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Sodium borohydrideHCID 4311764—
반응물4-(4-Fluorophenyl)pyridineHCID 15544371—
용매AcetoneHCID 180—
생성물1-Benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridineHCID 1006151078.2%

반응 단계

Benzyl bromide (52.4 mL, 441 mmol) was added to a solution of 4-(4-fluorophenyl)pyridine (Description 14, 50.87 g, 294 mmol) in acetone (500 mL) and the mixture was heated under reflux for 3 days. The mixture was cooled to room temperature and the solid was collected, washed with acetone and diethyl ether and dried in vacuo. The solid was dissolved in methanol (400 mL) and water (100 mL), cooled to 0° C. and sodium borohydride (20.6 g, 542 mmol) was added in portions. The mixture was stirred at room temperature for 1 hour, then heated to reflux for 18 hours. The mixture was cooled and the solvent was evaporated under reduced pressure. Dichloromethane (300 mL) and water (200 mL) were added and the layers were separated. The organic layer was dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound as a light brown oil (61.5 g, 78%). m/z (ES+) 268 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06953792B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-7ab6881b6326435088c982c926dd085b
출처 메모uspto-grants-2005_10