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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388471Generated: November 3, 2026

Acetate → Ethyl 2-(2-aminothiazol-4-yl)-2-methoxyiminoacetate

https://huagongshe.com/reaction/1388471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantSodium BicarbonateHCID 516892—
ReactantThioureaHCID 2723790—
ReactantEthyl 4-chloro-2-(methoxyimino)-3-oxobutanoateHCID 3017525—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductEthyl 2-(2-aminothiazol-4-yl)-2-methoxyiminoacetateHCID 58109168.5%

Reaction Steps

Ethyl 2-methoxyimino-4-chloroacetoacetate (syn isomer) (50 g.) was added over 3 minutes with stirring at ambient temperature to a solution of thiourea (18.4 g.) and solution acetate (19.8 g.) in a mixture of methanol (250 ml.) and water (250 ml.). After stirring for 35 minutes at 40° to 45° C., the reaction mixture was cooled with ice and adjusted to pH 6.3 with a saturated aqueous solution of sodium bicarbonate. After stirring for 30 minutes at the same temperature, precipitates were collected by filtration, washed with water (200 ml.) and then with diisopropyl ether (100 ml.), and dried to give colorless crystals of ethyl 2-methoxyimino-2-(2-amino-1,3-thiazol-4-yl)acetate (syn isomer) (37.8 g.), mp 161° to 162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431643
Source datasetuspto-grants-1984_02
ORD IDord-af5895842fcf4a03a087b98eb3e636ea
Source noteuspto-grants-1984_02