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HRID 28183作成日:2026年10月24日

Hydrogen Bromide → 3,4-Methylenedioxybenzylthio-acetic acid

https://huagongshe.com/ja/reaction/28183

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Bicarbonate IonHCID 769—
反応物Diisopropyl EtherHCID 7914—
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 allowed to cool. Crystals of thiouronium salt appear; these are filtered off and suction-drained. The precipitate thus obtained is introduced into a 500 ml three-necked flask together 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. The whole is then heated under reflux for half an hour, after which it is cooled. The mixture is acidified with 3N HCl, the precipitate obtained is redissolved in a dilute (sodium) bicarbonate solution, and the solution is washed with methylene chloride, filtered over charcoal and again acidified with 3N HCl so as to precipitate 3,4-methylenedioxybenzylthio-acetic acid, which is filtered off. After recrystallisation from a 1:1 (volume/volume) mixture of diisopropyl ether and petroleum ether, 18.2 g (40% yield) of the said acid (instantaneous melting point=87° C.) are collected.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04225617
出典データセットuspto-grants-1980_09
ORD IDord-b39752b53b1947aa81e876ffdc1c2b70
出典メモuspto-grants-1980_09