Acetic Acid → 2,2,2-Trichloroethyl 2-acetoxymethyl-2-methyl-6-(2-phenylacetamido)-penam-3-carboxylate

HRID 1438783Notes

Reaction equation

HRID 1438783 reaction equation
[C:1]([OH:4])(=[O:3])[CH3:2].Br[CH2:6][C:7]1([CH3:33])[CH:11]([C:12]([O:14][CH2:15][C:16]([Cl:19])([Cl:18])[Cl:17])=[O:13])[N:10]2[C:20](=[O:32])[CH:21]([NH:22][C:23](=[O:31])[CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C@H:9]2[S:8]1>C(Cl)Cl.C([O-])(=O)C.[Ag+]>[Cl:17][C:16]([Cl:19])([Cl:18])[CH2:15][O:14][C:12]([CH:11]1[N:10]2[C:20](=[O:32])[CH:21]([NH:22][C:23](=[O:31])[CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C@H:9]2[S:8][C:7]1([CH2:6][O:4][C:1](=[O:3])[CH3:2])[CH3:33])=[O:13]

Participants

5

Procedure

Acetic acid (2 ml) was added to a solution of 2,2,2-trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate (0.54 g) in methylene chloride (10 ml). And to this solution was added silver acetate (0.34 g) water stirring at room temperature and then the mixture was stirred for 2.5 hours. After the reaction was completed, the reaction mixture was filtered under reduced pressure and the filtrate was washed with 5% hydrochloric acid and then filtered again. The oily residue was crystallized by treating with ether and the crystals were collected by filtration and then dried to give colorless needles of 2,2,2-trichloroethyl-2-acetoxymethyl-2-methyl-6-(2-phenylacetamido)-penam-3-carboxylate (0.21 g), mp 116° to 118° C.

Workup

  1. filtrationthe reaction mixture was filtered under reduced pressure
  2. washthe filtrate was washed with 5% hydrochloric acid
  3. filtrationfiltered again
  4. customThe oily residue was crystallized
  5. additionby treating with ether
  6. filtrationthe crystals were collected by filtration
  7. customdried

Sources & evidence

ORD record
ord-3a1e5534082946a9a8a58528ba5c7148
Source dataset
uspto-grants-1977_11
Patent number
US04056521

Reaction notes

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