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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463859Generated: October 27, 2026

Benzene → Ethyl 2-hydroxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate

https://huagongshe.com/reaction/463859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantThioacetamideHCID 2723949—
ReactantHCID 178472904HCID 178472904—
SolventTriethylamineHCID 8471—
ProductEthyl 2-hydroxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetateHCID 73178131—

Reaction Steps

A mixture of ethyl 2-hydroxyimino-4-bromoacetoacetate (a mixture of syn and anti isomers) (22.0 g.), thioacetamide (7.5 g.) and benzene (100 ml.) was refluxed for 3 hours. After cooling triethylamine (10 g.) was added thereto and the mixture was stirred for 1 hour. An insoluble material was filtered off and the filtrate was concentrated under reduced pressure to give ethyl 2-hydroxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate (a mixture of syn and anti isomers) (8.6 g.). This substance was subjected to column chromatography on silica gel (80 g.) using benzene as developing solvent. Firstly the eluate containing anti isomer was eluted, collected and concentrated to give ethyl 2-hydroxyimino-2-(2-methyl-1,3-thiazol-4-yl)acetate (anti isomer) (2.5 g.), mp 90° to 92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544653
Source datasetuspto-grants-1985_10
ORD IDord-0af38b16161a40849145bf51432931cf
Source noteuspto-grants-1985_10