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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583273Generated: October 27, 2026

Carbon Disulfide → 3-{2-[(2-Hydroxyethyl)sulfanyl]ethyl}-4-methyl-1,3-thiazole-2(3H)-thione

https://huagongshe.com/reaction/1583273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantChloroacetoneHCID 6571—
ReactantTriethylamineHCID 8471—
Reactant2-((2-Aminoethyl)thio)ethanolHCID 90457—
SolventEthanolHCID 702—
Product3-{2-[(2-Hydroxyethyl)sulfanyl]ethyl}-4-methyl-1,3-thiazole-2(3H)-thioneHCID 20260303—

Reaction Conditions

Temperature0 °C

Reaction Steps

In 500 ml of ethanol, 24.2 g of (2) and 24.7 ml of triethylamine were dissolved and cooled to 0° C. Thereto, 16.8 g of carbon disulfide was added dropwise. The resulting mixture was allowed to stand for 2 hours at a room temperature and further, for an additional 30 minutes at 50° C. to conduct the reaction. Then, the reaction mixture was cooled to 0° C. again. Thereto, 19.4 g of chloroacetone was added dropwise. The reaction was run by keeping the temperature of the reactionsystem at a room temperature for 1 hour and further, at 40° C. for an additional 2 hours. At the conclusion of the reaction, the solvent was removed by distillation under reduced pressure, and water was added to the residue. The reaction product was extracted with ethyl acetate, washed with water three times, and dried over anhydrous sodium sulfate. Upon the removal of ethyl acetate from the extract by distillation, (1) was obtained as an oily sub stance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551419
Source datasetuspto-grants-1985_11
ORD IDord-33c03bfc644b4b1c85cfe0d37875d43b
Source noteuspto-grants-1985_11