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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1005093생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1005093

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물4-(4-Fluorophenyl)-1,2,3,6-tetrahydropyridine hydrochlorideHCID 197747—
용매EthanolHCID 702—
생성물1-Benzyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridineHCID 1006151071.1%

반응 단계

13.8 g (100 mmol) of potassium carbonate were added to a solution of 10.0 g (46.8 mmol) of 4-(4-fluoro-phenyl)-1,2,3,6-tetrahydro-pyridine hydrochloride in 400 ml of ethanol and the reaction mixture was subsequently heated to reflux temperature. A solution of 5.8 ml (49 mmol) of benzyl bromide in 100 ml of ethanol was added dropwise within one hour and thereafter the mixture was stirred at this temperature for a further 1 hour. The reaction mixture was cooled to room temperature and filtered, the filtrate was extracted with water and ethyl acetate and finally the organic phase was dried over magnesium sulphate. After evaporation in a water-jet vacuum the crude product obtained was chromatographed on silica gel with hexane and ethyl acetate as the eluent. There were obtained 8.90 g (71% of theory) of 1-benzyl-4-(4-fluoro-phenyl)-1,2,3,6-tetrahydro-pyridine; MS: 267 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06051712
출처 데이터셋uspto-grants-2000_04
ORD IDord-aeadaa423c97444aa6f42b28a02de35c
출처 메모uspto-grants-2000_04