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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983674Generated: October 26, 2026

Toluene → 4-Phenyl-2-[acetylthio-methyl]butyric acid

https://huagongshe.com/reaction/983674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiethyl EtherHCID 3283—
ReactantPiperidineHCID 8082—
Reactant2-Thiopheneacetic acidHCID 15970—
Reactant2-Methylene-4-phenylbutyric acidHCID 13817411—
Product4-Phenyl-2-[acetylthio-methyl]butyric acidHCID 1010625481%

Reaction Conditions

Temperature5 °C

Reaction Steps

A 250 mL round bottomed flask, fitted with a Teflon magnetic stirring bar and a reflux condenser, was filled with 150 mL of toluene, 0.5 mL piperidine and 8.6 g (49 mmole) of 4-phenyl-2-methylenebutyric acid. Then 4.1 g (54 mmole) of thiolacetic acid was added to the solution and the mixture heated to reflux for 8 hours under nitrogen. 1H-NMR analysis of the reaction mixture indicated some starting material remained. Another 1 g of thiolacetic acid was added and the mixture stirred at reflux for an additional 4 hours. By 1H-NMR, all of the starting material was seen to have reacted. The solution was cooled to 5° C., and 100 mL of ether added to the mixture. The excess thiolacetic acid was removed by extraction (3×50 mL 2% sodium bicarbonate). Then 50 mL of 1N HCl was added to the organic layer and the solution shaken vigorously. The organic layer was separated and dried over MgSO4. The solution was filtered and the solvent removed under reduced pressure. Recovered 10.0 g of product (81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864383B2
Source datasetuspto-grants-2005_03
ORD IDord-67aa0b6ec3fc454fbeabea672706ad6a
Source noteuspto-grants-2005_03