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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197339Generated: October 25, 2026

Water → 3-(Prop-2-ynylthio)propionic acid

https://huagongshe.com/reaction/1197339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Mercaptopropionic AcidHCID 6514—
ReactantPropargyl bromideHCID 7842—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product3-(Prop-2-ynylthio)propionic acidHCID 19373376—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-mercaptopropionic acid (15 ml) in dry dimethylformamide (250 ml) was stirred at 0°, under nitrogen. Sodium hydride (10.2 g; 80% dispersion in oil) was added carefully and the mixture was stirred at 40° for 1 hour. The mixture was cooled to 0° C. and propargyl bromide (60 g; 80% in toluene) was added dropwise. The mixture was stirred at 20° for 3 hours and then at 80° for 1 hour. The mixture was cooled and poured into water. The aqueous mixture was extracted with diethyl ether, and the extracts washed with water and dried over anhydrous magnesium sulphate. The solvent was removed in vacuo. The resulting oil (30 g) (mainly prop-2-ynyl 3-(prop-2-ynylthio(propionate) was added to a solution of sodium hydroxide (8.0 g) in water (100 ml) and methanol (100 ml) and the mixture was stirred at 20° for 24 hours. The mixture was extracted with diethyl ether and the aqueous solution was acidified with hydrochloric acid. The acidic mixture was extracted with diethyl ether and the ethereal extracts were dried over anhydrous magnesium sulphate. The solvent was removed in vacuo. 3-(Prop-2-ynylthio) propionic acid was obtained as a red oil (12.0 g) and was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116862
Source datasetuspto-grants-1992_05
ORD IDord-b391906a65ac4c03b673066b6d0c770a
Source noteuspto-grants-1992_05