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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65519Generated: October 27, 2026

Ethyl Acetate → 2-(2-aminothiazol-4-yl)thioacetic acid-S-ethyl ester

https://huagongshe.com/reaction/65519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantThioureaHCID 2723790—
Reactant4-bromo-3-oxothiobutyric acid-S-ethyl esterHCID 13821657—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product2-(2-aminothiazol-4-yl)thioacetic acid-S-ethyl esterHCID 1382165465.5%

Reaction Steps

In 7.0 ml of N,N-dimethylacetamide was dissolved 2.25 g of the 4-bromo-3-oxothiobutyric acid-S-ethyl ester obtained in Referential Example 4-(1), and 1.14 g of thiourea was added to the resulting solution with ice-cooling, after which the resulting mixture was subjected to reaction at room temperature for 1 hour. The reaction mixture was introduced into a mixed solvent of 50 ml of ethyl acetate and 50 ml of water, and the pH was adjusted to 6.0 with sodium hydrogencarbonate. Then, the organic layer was separated, washed with two 50-ml portions of water and with 50 ml of saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. Then the solvent was removed by distillation under reduced pressure. The residue obtained was recrystallized from 20 ml of ethyl acetate to obtain 1.32 g (yield, 65.5%) of 2-(2-aminothiazol-4-yl)thioacetic acid-S-ethyl ester having a melting point of 76°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614819
Source datasetuspto-grants-1986_09
ORD IDord-5b30943ef83441d39a27c23d957e3439
Source noteuspto-grants-1986_09