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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131988생성일: 2026년 10월 27일

Hydrochloric Acid → Tolperisone Hydrochloride

https://huagongshe.com/reaction/131988

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,3-DioxolaneHCID 12586—
반응물p-MethylpropiophenoneHCID 21429—
반응물Piperidine, hydrochloride (1:1)HCID 2723721—
반응물Calcium ChlorideHCID 5284359—
생성물Tolperisone HydrochlorideHCID 92965—

반응 조건

온도84.5 °C

반응 단계

In a 3-L-three neck flask with a reflux condenser, a calcium chloride drying tower, and under an argon flow, 200 ml of 1,3-dioxolane and 146.2 ml of 4-methylpropiophenone are subjected to agitation and then there is added through a funnel 100 g piperidine hydrochloride and 4.0 ml of 33% aqueous hydrochloric acid. The powder in the funnel is washed afterwards with 20 ml 1,3-dioxolane, and the stirrer is switched on in the reaction flask. The reaction mixture is purged once with argon and stirred at 100-105° C. bath temperature (83-86° C. interior temperature). The white precipitate dissolves after approximately 15-16 hours. After 18-20 hours the thin layer chromatogram shows no more piperidine. After 24 hours the heating is switched off and the oil bath is removed and while still warm, and under vigorous stirring to the clear reaction solution, there is added 800 ml ethyl acetate and then the solution is cooled to ambient temperature and then further treated with 400 ml methyl tert-butylether (MTBE). The resulting precipitate is agitated at α to 10° C. for an additional 2 hours, and then filtered off over a glass filter (Po-3) and washed afterwards twice with 200 ml MTBE each time. The substance is dried in the vacuum drying oven at 75-80° C. and 20-40 mbar for 16 to 24 hours.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07385060B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-d216d59b83b949c5b5bf552e7fcd8c9b
출처 메모uspto-grants-2008_06