Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155157Generated: November 2, 2026

Thiourea → Ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate hydrobromide

https://huagongshe.com/reaction/1155157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
ReactantButanoic acid, 4-bromo-2-(methoxyimino)-3-oxo-, ethyl esterHCID 54053279—
SolventEthanolHCID 702—
ProductEthyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate hydrobromideHCID 73668749—

Reaction Steps

A solution of ethyl 2-methoxyimino-4-bromoacetoacetate (a mixture of syn and anti isomers) (17.4 g.) and thiourea (5.4 g.) in ethanol (100 ml.) was refluxed for 4 hours. The reaction mixture was allowed to stand in a refrigerator to precipitate crystals. The crystals were collected by filtration, washed with ethanol and dried to give ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate hydrobromide (anti isomer) (9.5 g.). The filtrate and the washings were put together and concentrated under reduced pressure. Water (100 ml.) was added to the residue and the mixture was washed with ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04299829
Source datasetuspto-grants-1981_11
ORD IDord-6d636eafaf48447bb21a71ac6646d0c3
Source noteuspto-grants-1981_11