Réaction #94921

Équation de réaction

trimethylchlorosilane

sodium cephalothin

monosilyltrifluoroacetamide

phenylacetyl chloride

→

7-(phenylacetyl-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid

Solvants

Conditions de réaction

Traitement

1. 1
   Autrefitted with a drying tube
2. 2
   AutreThe volatiles are evaporated
3. 3
   Autreto afford a residue which
4. 4
   workup.DISSOLUTIONis dissolved in 100 ml
5. 5
   Lavageof ethyl acetate and washed three times with water
6. 6
   SéchageThe ethyl acetate layer is dried over magnesium sulfate
7. 7
   Filtrationfiltered
8. 8
   Autrethe solution evaporated in vacuo to a residue
9. 9
   AutreThe residue is triturated with chloroform
10. 10
    Autreany insolubles are removed by filtration
11. 11
    Autrethe product precipitated from the filtrate with hexane

Mode opératoire

A suspension of sodium cephalothin (3.36 g.) in anhydrous alcohol-free chloroform (20 ml.) is silylated by the addition of trimethylchlorosilane (2.2 ml.). After stirring for 30 minutes, monosilyltrifluoroacetamide (5.0 ml.) and phenylacetyl chloride (4.0 ml.) are added and the mixture is then heated to 45° C. for two days under a condenser fitted with a drying tube. The volatiles are evaporated to afford a residue which is dissolved in 100 ml. of ethyl acetate and washed three times with water. The ethyl acetate layer is dried over magnesium sulfate, filtered and the solution evaporated in vacuo to a residue. The residue is triturated with chloroform, any insolubles are removed by filtration and the product precipitated from the filtrate with hexane. This procedure is followed two more times. The 7-(phenylacetyl-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.

Source