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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486899Generated: October 27, 2026

Thioglycolic Acid → [{(6-Methyl-1,3-benzodioxol-5-yl)methyl}thio]acetic acid

https://huagongshe.com/reaction/486899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioglycolic AcidHCID 1133—
ReactantChloroformHCID 6212—
ReactantSodium HydroxideHCID 14798—
Reactant5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxoleHCID 10559416—
SolventEthanolHCID 702—
Product[{(6-Methyl-1,3-benzodioxol-5-yl)methyl}thio]acetic acidHCID 1451491520.5%

Reaction Steps

A suspension of 6.0 g of 5-chloromethyl-6-methyl-1,3-benzodioxole, 6.0 g of mercaptoacetic acid and 6.5 g of sodium hydroxide in 130 ml of 50% hydrous ethanol was heated under reflux for 1 h. The reaction mixture was concentrated. Water was added thereto and the mixture was washed with ethyl acetate. The aqueous layer was acidified with 1Nhydrochloric acid. After extraction with chloroform, the extract was dried over magnesium sulfate. The solvent was distilled off and the product was isolated according to silica gel column chromatography (chloroform). The crystals thus obtained were recrystallized from diisopropyl ether to obtain 1.6 g of the intended compound in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292901
Source datasetuspto-grants-1994_03
ORD IDord-2cdbc011d78d4871827a72c28ac197c6
Source noteuspto-grants-1994_03