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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486902Generated: October 27, 2026

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

https://huagongshe.com/reaction/486902

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 numberUS05292901
Source datasetuspto-grants-1994_03
ORD IDord-b5d3b36d1eb444e981b16ace5af2720b
Source noteuspto-grants-1994_03