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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1476019생성일: 2026년 10월 26일

Benzyl Chloride → Benzethonium Chloride

https://huagongshe.com/reaction/1476019

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물Methyl Isobutyl KetoneHCID 7909—
반응물Ethanamine, N,N-dimethyl-2-[2-[4-(1,1,3,3-tetramethylbutyl)phenoxy]ethoxy]-HCID 79514—
용매CyclohexaneHCID 8078—
생성물Benzethonium ChlorideHCID 8478—

반응 단계

170.0 g of p-tert-octyl phenoxy ethoxy ethyl dimethylamine was added to a 1 L four-necked reaction flask, to which were sequentially added 100.2 g of methyl isobutyl ketone and 126.6 g of benzyl chloride. The reaction mixture was heated to reflux. The reaction was carried out for 2 hours. Then, 168.2 g of cyclohexane was added slowly. The flask was cooled to carry out crystallization. 156.8 g of a white solid was collected. The content of benzethonium chloride was 99.2% determined by titration according to the method described on page 247 of the United States Pharmacopeia USP29. The measured melting point was from 159.0 to 162.0° C. As calculated with reference to p-tert-octyl phenol, an overall yield of the three steps was less than 15%, which is remarkably far from that obtained by using a phase transfer catalyst. Thus, it does not have a practical application value.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09018418B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-69d54acfe72842e4a2738f575a5ce4ae
출처 메모uspto-grants-2015_04