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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080867Generated: October 31, 2026

Chloroacetyl chloride → HCID 86735835, compound

https://huagongshe.com/reaction/1080867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 86735836HCID 86735836—
SolventDimethylacetamideHCID 31374—
ProductHCID 86735835HCID 8673583579%

Reaction Steps

To a solution of 2.43 g of ethyl α-ethoxyimino-2-aminothiazol-4-ylacetate hydrobromide in 25 ml of anhydrous N,N-dimethylacetamide is added 1.43 g of chloroacetyl chloride under cooling and stirring. The solution is stirred for 30 minutes under ice-cooling and then for 30 minutes at room temperature. To the reaction mixture is added 150 ml of ethyl acetate and the mixture is repeatedly washed with saturated sq. NaCl solution. The ethyl acetate layer is dried over anhydrous magnesium sulfate, and subjected to the distillation of the solvent under reduced pressure. To the residue is added water to precipitate solid material. The solid is collected by filtration and dried. The procedure gives 1.90 g of ethyl α-ethoxyimino-2-(chloroacetamino)thiazol-4-ylacetate. Yield 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583216
Source datasetuspto-grants-1996_12
ORD IDord-50d1f686c39c425ca8d69fec6429783b
Source noteuspto-grants-1996_12