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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2285939생성일: 2026년 10월 24일

Hydrogen Bromide → 3,4-Methylenedioxybenzylthio-acetic acid

https://huagongshe.com/ko/reaction/2285939

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물Chloroacetic AcidHCID 300—
반응물Hydrochloric AcidHCID 313—
반응물Piperonyl alcoholHCID 10322—
반응물Sodium HydroxideHCID 14798—
반응물ThioureaHCID 2723790—
반응물HCID 178512448HCID 178512448—
용매Bicarbonate IonHCID 769—
용매WaterHCID 962—
생성물3,4-Methylenedioxybenzylthio-acetic acidHCID 17852616752.8%

반응 조건

온도60 °C

반응 단계

A solution of 18.24 g (0.24 mol) of thiourea in 104 ml of 48% strength hydrobromic acid and 20 ml of water is introduced into a one liter three-necked flask equipped with a magnetic stirrer and a condenser. The mixture is heated to 60° C. and 30.4 g (0.2 mol) of piperonyl alcohol are introduced. The temperature is raised to 95° C. and the mixture is left to cool. Crystals of the thiouronium salt appear; these are filtered off and dried. The precipitate thus obtained is introduced into a 500 ml three-necked flask with 60 ml of sodium hydroxide solution. The mixture is heated to 70° C. and 15.6 g (0.164 mol) of chloroacetic acid in 30 ml of water are added dropwise. Thereafter the whole is heated under reflux for half an hour and then cooled. The mixture is acidified with 3 N HCl, the precipitate obtained is redissolved in a dilute bicarbonate solution, and the solution is washed with methylene chloride, filtered over charcoal and acidified once more with 3 N HCl in order to precipitate 3,4-methylenedioxybenzylthio-acetic acid, which is filtered off. After recrystallisation from a diisopropyl ether/petroleum ether mixture (1:1 v/v), 18.2 g (yield 40%) of the said acid are collected (instantaneous melting point=87° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04325964
출처 데이터셋uspto-grants-1982_04
ORD IDord-c60e6622d2a04554ad1ff810928b137b
출처 메모uspto-grants-1982_04