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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259732Generated: October 31, 2026

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

https://huagongshe.com/reaction/2259732

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 and the mixture was heated under reflux for 4 h. The solvent was distilled off and the pH of the residue was adjusted to 10 with 1N aqueous sodium hydroxide solution. After washing with ethyl acetate, 4N hydrochloric acid was added thereto under cooling with ice to acidity the aqueous layer. After extraction with chloroform, the extract was washed with water and dried over anhydrous magnesium sulfate. It was filtered and the filtrate was concentrated. The crystals thus formed were recrystallized form diisopropyl ether to obtain 62.70 g of the intended compound in the form of colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475024
Source datasetuspto-grants-1995_12
ORD IDord-106998c6466a4a68b4434f47472975fc
Source noteuspto-grants-1995_12