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HRID 2285939作成日:2026年10月25日

Hydrogen Bromide → 3,4-Methylenedioxybenzylthio-acetic acid

https://huagongshe.com/reaction/2285939

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物Chloroacetic AcidHCID 300—
反応物Hydrochloric AcidHCID 313—
反応物Piperonyl alcoholHCID 10322—
反応物Sodium HydroxideHCID 14798—
反応物ThioureaHCID 2723790—
反応物HCID 178512448HCID 178512448—
溶媒Bicarbonate IonHCID 769—
溶媒WaterHCID 962—
生成物3,4-Methylenedioxybenzylthio-acetic acidHCID 17852616752.8%

反応条件

温度60 °C

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04325964
出典データセットuspto-grants-1982_04
ORD IDord-c60e6622d2a04554ad1ff810928b137b
出典メモuspto-grants-1982_04