تفاعل #65627

معادلة التفاعل

vinyl tri-n-butylstannane

diphenylmethyl 7-phenoxyacetamido-3-[(fluorosulfonyl)oxy] -3-cephem-4-carboxylate

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title compound

المردود 88.8%

Diphenylmethyl 7-Phenoxyacetamido-3-vinyl-3-cephem-4-carboxylate

المردود 88.8%

المذيبات

ethyl acetate

1-methyl-2-pyrrolidinone

ظروف التفاعل

المعالجة

1. 1
   workup.STIRRINGto stir for 10 minutes
2. 2
   غسيلwashed with 3×20 mL of water
3. 3
   تجفيفThe organic fraction was dried over magnesium sulfate
4. 4
   تركيزthen concentrated
5. 5
   ترشيحThe crude brown residue was purified by flash filtration through a pad of silica gel (W. R. Grace, 951W) first with dichloromethane (50 mL)
6. 6
   أخرىto remove the residual stannane
7. 7
   تركيزwith 10% ethyl acetate in dichloromethane (75 mL), which upon concentration

الإجراء التجريبي

A solution of palladium (II) acetate (3.6 mg, 0.016 mmol, 0.1 eq.) in 1-methyl-2-pyrrolidinone (2 mL) was treated with vinyl tri-n-butylstannane (58.4 mL, 0.2 mmol, 1.2 eq.) under an inert atmosphere and allowed to stir for 3 minutes. The resulting dark suspension was then treated with diphenylmethyl 7-phenoxyacetamido-3-[(fluorosulfonyl)oxy] -3-cephem-4-carboxylate (100.0 mg, 0.16 mmol, 1.0 eq.) in one portion and the reaction mixture was allowed to stir for 10 minutes. The reaction mixture was diluted with ethyl acetate and washed with 3×20 mL of water. The organic fraction was dried over magnesium sulfate then concentrated. The crude brown residue was purified by flash filtration through a pad of silica gel (W. R. Grace, 951W) first with dichloromethane (50 mL) to remove the residual stannane and then with 10% ethyl acetate in dichloromethane (75 mL), which upon concentration furnished 74.8 mg (85%) of the title compound as a white solid.

المصدر