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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66644Generated: October 25, 2026

Chlorotrimethylsilane → 7-(Di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/66644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2-Thiopheneacetyl chlorideHCID 162362—
ReactantCephalothin SodiumHCID 23675321—
ReactantMonosilyltrifluoroacetamideHCID 123231972—
SolventChloroformHCID 6212—
Product7-(Di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acidHCID 70541217—

Reaction Conditions

Temperature45 °C

Reaction Steps

A suspension of sodium cephalothin (1.18 g.) in anhydrous alcohol-free chloroform (10 ml.) is silylated by the addition of trimethylchlorosilane (1.1 ml.). After stirring for 30 minutes, monosilyltrifluoroacetamide (2.5 ml.) and 2-thienylacetyl chloride (2.0 ml.) are added to the suspension which is then heated to 45° C. The mixture is allowed to remain at this temperature for two days and then evaporated in vacuo to a residue which is dissolved in ethyl acetate (50 ml.) and washed three times with water. The ethyl acetate layer is dried over magnesium sulfate, filtered and the filtrate evaporated in vacuo to obtained a residue. The residue is dissolved in chloroform and precipitated with hexane three times, each time discarding the supernatent liquid. The 7-(di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid is obtained in a solvent-free form by freeze-drying from a solution in benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342757
Source datasetuspto-grants-1982_08
ORD IDord-5bd39d5c12d448c8a6d7ff4fbd656c60
Source noteuspto-grants-1982_08