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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328062Generated: October 30, 2026

Dichloroacetyl chloride → 7-Dichloroacetamido-3-(1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/328062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloroacetyl chlorideHCID 6593—
ReactantBistrimethylsilylacetamidHCID 11708267—
Reactant7-Amino-3-(1,3,4-thiadiazol-2-ylthiomethyl)-3cephem-4-carboxylic acidHCID 12889187—
SolventDichloromethaneHCID 6344—
Product7-Dichloroacetamido-3-(1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acidHCID 7063214380.6%

Reaction Steps

7-Amino-3-(1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acid (6.61 g) was suspended in methylene chloride (60 ml) and bis(trimethylsilyl)acetamide was added to the suspension to give a solution. A solution of dichloroacetyl chloride (3.24 g) in methylene chloride (10 ml) was added to the solution obtained above at -20° C under stirring. The mixture was stirred at the same temperature for 20 minutes. Methylene chloride was distilled off under reduced pressure after addition of a little water. Water was added to the residue and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride and dried, and the solvent was distilled off under reduced pressure. The residue was pulverized by treating with ether and precipitates were collected by filtration to give 7-dichloroacetamido-3-(1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acid (7.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04016160
Source datasetuspto-grants-1977_04
ORD IDord-1f7b5ce0e0bc4e2cbba634fe398c6d0e
Source noteuspto-grants-1977_04