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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 986444생성일: 2026년 10월 24일

Water → 3-[p-(3-Chloropropionyl)benzyl]pyridine

https://huagongshe.com/ko/reaction/986444

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-Chloropropionyl chlorideHCID 69364—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물3-Benzylpyridine hydrochlorideHCID 12210545—
용매DichloromethaneHCID 6344—
생성물3-[p-(3-Chloropropionyl)benzyl]pyridineHCID 2014863786.6%

반응 단계

In 15 ml of methylene chloride was suspended 8.1 g of anhydrous aluminum chloride, and 3.0 ml of 3-chloropropionyl chloride was added to the suspension with ice-cooling, after which 5.0 g of 3-benzylpyridine hydrochloride was added in small portions to the resulting mixture over 30 minutes. The resulting mixture was subjected to reaction at room temperature for one hour, and then the reaction mixture was added to 30 ml of iced water. The crystals thus precipitated were collected by filtration, and suspended in a mixture of 50 ml of ethyl acetate and 30 ml of water, after which the resulting suspension was neutralized with sodium hydrogen-carbonate with ice-cooling. Insolubles were removed by filtration, and the organic layer of the filtrate was separated, washed with 10 ml of a saturated aqueous sodium chloride solution, and then dried over anhydrous magnesium sulfate, after which the solvent was removed by distillation under reduced pressure to obtain 5.5 g (yield 86.6%) of pale yellow, oily 3-[p-(3-chloropropionyl)benzyl]pyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04713387
출처 데이터셋uspto-grants-1987_12
ORD IDord-c987ac0eb19b4ecdbc4ba79814afb32b
출처 메모uspto-grants-1987_12