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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 236568생성일: 2026년 10월 25일

Potassium Carbonate → alpha-Ethyl-alpha-(4-chlorophenyl)-4-[3-(di-n-propylamino)-propoxy]-benzylalcohol

https://huagongshe.com/reaction/236568

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Dipropylaminopropyl chlorideHCID 12333917—
반응물alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매Ethyl AcetateHCID 8857—
생성물alpha-Ethyl-alpha-(4-chlorophenyl)-4-[3-(di-n-propylamino)-propoxy]-benzylalcoholHCID 20216260—

반응 단계

13.1 g. of α-ethyl-α-(4-chlorophenyl)-4-hydroxy-benzylalcohol, 14 g. of anhydrous potassium carbonate, 9.8 g. of dipropylaminopropyl chloride and 0.85 g. of tetrabutyl ammonium hydrogensulfate in 135 ml. of ethyl acetate are slightly boiled for 20 hours, under stirring. After cooling the mixture, the solvent is evaporated in vacuo. To the residue water and benzene are added. The phases are separated, the benzene solution is washed with water, dried over anhydrous potassium carbonate, filtered and evaporated. The residue is purified by vacuum fractionation. 13.8 g. of the desired end product are obtained, boiling at 198° to 200° C./1.33 Pa.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04645779
출처 데이터셋uspto-grants-1987_02
ORD IDord-207e32b5a3714d40af02fe0ad4959c98
출처 메모uspto-grants-1987_02