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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388465Generated: November 3, 2026

Thioacetamide → Ethyl 2-methoxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate

https://huagongshe.com/reaction/1388465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioacetamideHCID 2723949—
ReactantButanoic acid, 4-bromo-2-(methoxyimino)-3-oxo-, ethyl esterHCID 54053279—
SolventEthanolHCID 702—
ProductEthyl 2-methoxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetateHCID 53983477—

Reaction Conditions

Temperature50 °C

Reaction Steps

Thioacetamide (3.8 g.) was added to a solution of ethyl 2-methoxyimino-4-bromoacetoacetate (a mixture of syn and anti isomers) (12.6 g.) in ethanol (50 ml.) and the mixture was stirred for 5 hours at 50° C. Ethanol was distilled off under reduced pressure and water was added to the residue. The resulting mixture was extracted with ethyl acetate. The extract was in turn washed with water, a sodium bicarbonate aqueous solution and a saturated sodium chloride aqueous solution and dried over magnesium sulfate. The solvent was distilled off under reduced pressure to give ethyl 2-methoxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate (a mixture of syn and anti isomers) (9.0 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431643
Source datasetuspto-grants-1984_02
ORD IDord-4cf152d9e5104313ba16701a31b1015e
Source noteuspto-grants-1984_02