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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195309Generated: November 1, 2026

Thioglycolic Acid → [{2-(1,3-Benzodioxol-5-yl)-2-propyl}thio]acetic acid

https://huagongshe.com/reaction/1195309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioglycolic AcidHCID 1133—
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
Reactant2-(Benzo[d][1,3]dioxol-5-yl)propan-2-olHCID 11819632—
SolventBenzeneHCID 241—
Product[{2-(1,3-Benzodioxol-5-yl)-2-propyl}thio]acetic acidHCID 1451490745.8%

Reaction Steps

600 ml of benzene, 59.5 g of mercaptoacetic acid and a catalytic amount of D-10-camphorsulfonic acid were added to 97 g of 2-(1,3-benzodioxol-5-yl)-2-propanol. The obtained mixture was heated under reflux for 4 hours and distilled to remove the solvent. The pH of the residue was adjusted to 10 with a 1N aqueous solution of sodium hydroxide. The resulting mixture was washed with ethyl acetate. 4N hydrochloric acid was added to the mixture under cooling with ice to acidify the aqueous layer. The resulting mixture was extracted with chloroform. The organic layer was washed with water, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated to obtain a crude crystal. This crude crystal was recrystallized from diisopropyl ether to obtain 62.70 g of the title compound as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110956
Source datasetuspto-grants-1992_05
ORD IDord-54e507e52c7f404aaf8860f0bbfdf2b5
Source noteuspto-grants-1992_05