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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259788Generated: November 1, 2026

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

https://huagongshe.com/reaction/2259788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioglycolic AcidHCID 1133—
ReactantEthyl AcetateHCID 8857—
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
Reactant(6-Methyl-1,3-benzodioxol-5-yl)butan-1-olHCID 67784687—
SolventBenzeneHCID 241—
Product[{1-(6-Methyl-1,3-benzodioxol-5-yl)butyl}thio]acetic acidHCID 1451493154%

Reaction Steps

A solution of 5.6 g of (6-methyl-1,3-benzodioxol-5-yl)butan-1-ol, 4.8 g of mercaptoacetic acid and a catalytic amount of D-10-camphorsulfonic acid in 60 ml of benzene was heated under reflux for 3 hours, followed by the addition of ethyl acetate. The obtained mixture was washed with water and extracted with a 1N aqueous solution of sodium hydroxide. The aqueous layer was washed with ethyl acetate, acidified with 1N hydrochloric acid and extracted with chloroform. The organic layer was dried over magnesium sulfate and distilled to remove the solvent. The obtained residue was chromatographed over silica gel column and eluted with chloroform to obtain a colorless crystal. This crystal was recrystallized from isopropyl ether/hexane to obtain 4.1 g of the title compound as a colorless prismatic crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475024
Source datasetuspto-grants-1995_12
ORD IDord-cd42a87f26ff4563a74cb02f00d5b1da
Source noteuspto-grants-1995_12