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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486953Generated: October 30, 2026

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

https://huagongshe.com/reaction/486953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioglycolic AcidHCID 1133—
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% aqueous ethanol was heated under reflux for one hour and concentrated, followed by the addition of water. The mixture was washed with ethyl acetate. The aqueous layer was acidified with 1N hydrochloric acid and extracted with chloroform. The organic layer was dried over magnesium sulfate and distilled to remove the solvent. The residue was chromatographed over a silica gel column and eluted with chloroform to obtain a crude crystal. This crude crystal was recrystallized from diisopropyl ether to obtain 1.6 g of the title compound as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292901
Source datasetuspto-grants-1994_03
ORD IDord-0aa97f3bad604b8cb28a466dcb9d34c7
Source noteuspto-grants-1994_03