돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28990생성일: 2026년 10월 24일

Hydrochloric Acid → 1-(4-Bromophenethyl)pyrrolidine

https://huagongshe.com/ko/reaction/28990

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물TriethylamineHCID 8471—
반응물PyrrolidineHCID 31268—
반응물2-(4-Bromophenyl)ethanolHCID 72851—
용매DichloromethaneHCID 6344—
생성물1-(4-Bromophenethyl)pyrrolidineHCID 1217781080%

반응 단계

To a solution of 4-bromophenethyl alcohol (2.54 mmol) and p-toluenesulfonyl chloride (2.74 mmol) in anhydrous dichloromethane (5 mL) under nitrogen was added triethylamine (2.74 mmol) dropwise by syringe at room temperature. The reaction was stirred for 16 hours at room temperature. A white precipitate formed. 1N HCl solution (5 mL) was added to the suspension and the reaction became clear. The layers were separated and the organic layer was washed with saturated aqueous sodium bicarbonate solution (5 mL), dried over magnesium sulfate and concentrated in vacuo to give a white solid. To this crude product was added pyrrolidine (1 mL) under nitrogen and the reaction was stirred at 50° C. for 90 minutes. The reaction was cooled to room temperature and concentrated in vacuo. The resulting residue was dissolved in ethyl acetate (20 mL) and washed successively with water (20 mL) and saturated aqueous sodium bicarbonate solution (20 mL), dried over magnesium sulfate and concentrated in vacuo. Purification by silica gel chromatography (20-100% ethyl acetate/hexanes) afforded the title compound as a white solid (80%). ESMS [M+H]+: 254.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419988B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1fcbdb5101594c8f84d2d6ef52cb4bb2
출처 메모uspto-grants-2008_09