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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195265Generated: October 31, 2026

Sodium Hydroxide → 2-(1,3-Benzodioxol-5-yl)ethanethiol

https://huagongshe.com/reaction/1195265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantThioureaHCID 2723790—
Reactant3,4-Methylenedioxyphenethyl bromideHCID 12207224—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(1,3-Benzodioxol-5-yl)ethanethiolHCID 1581951295.5%

Reaction Steps

750 g of 5-(2-bromoethyl)-1,3-benzodioxole was dissolved in 1 l of ethanol. 312 g of thiourea was added to the solution and the mixture was heated under reflux on a boiling water bath for 2 h. The reaction mixture was cooled. A solution of 300 g of sodium hydroxide in 1 l of water was added thereto and the mixture was heated under reflux on a boiling water bath for 45 min. After cooling, 3 l of water was added thereto and the product was extracted with 5 l of ethyl acetate. The extract was washed with dilute hydrochloric acid. It was then washed with water until the washing became substantially neutral and dried over anhydrous sodium sulfate. The solvent was distilled off at 40° C. to obtain about 570 g of a faint yellow oil. It was purified according to column chromatography with about 3 kg of silica gel (hexane : benzene=2:1) to obtain 310 g of the intended compound in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110956
Source datasetuspto-grants-1992_05
ORD IDord-93f5c821c64d4e7e9712682d50704c24
Source noteuspto-grants-1992_05