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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486949Generated: October 27, 2026

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

https://huagongshe.com/reaction/486949

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 numberUS05292901
Source datasetuspto-grants-1994_03
ORD IDord-e2f9642b70ef488280af7e44c21ac864
Source noteuspto-grants-1994_03