Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325379Generated: October 25, 2026

Trichloroisocyanuric Acid → Ethyl (2-formamido-5-chlorothiazol-4-yl)glyoxylate

https://huagongshe.com/reaction/325379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroisocyanuric AcidHCID 6909—
ReactantEthyl 2-(formylamino)-alpha-oxo-4-thiazoleacetateHCID 2733245—
ReactantHCID 178473042HCID 178473042—
SolventDimethylformamideHCID 6228—
ProductEthyl (2-formamido-5-chlorothiazol-4-yl)glyoxylateHCID 14326717—

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of ethyl 2-(2-formylamino-1,3-thiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2formylimino-2,3-dihydro-1,3-thiazol-4-yl)glyoxylate, (6.9 g.) in dimethylformamide (40 ml.) was heated at 60° C. to produce a solution, and to the solution was dropwise added a solution of trichloroisocyanuric acid (2.8 g.) in dimethylformamide (10 ml.) over 15 minutes at the same temperature with stirring and then the mixture was further stirred for 1 hours at the same temperature. After the reaction, the reaction mixture was poured into ice-water (400 g.). The precipitates were collected by filtration, washed with water and then dried to give ethyl 2-(2-formylamino-5-chloro-1,3-thiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-formylimino-5-chloro-2,3-dihydro-1,3-thiazol-4-yl)glyoxylate, (7.1 g.), mp. 151° to 153° C. The remaining filtrate was extracted with ethyl acetate, and the extract was washed with water and then dried over magnesium sulfate. The solvent was distilled off from the extract to give further the same object compound (0.75 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04440766
Source datasetuspto-grants-1984_04
ORD IDord-95debc1b2d264f41ad032a21cea6022d
Source noteuspto-grants-1984_04