Trifluoroacetic acid → Methyl 7-phthalimido-3-methylenecepham-4-carboxylate 1-oxide
Reaction equation
[CH3:1][C:2](=[CH2:27])[CH:3]([N:8]1[C:11](=[O:12])[CH:10]([N:13]2[C:17](=[O:18])[C:16]3=[CH:19][CH:20]=[CH:21][CH:22]=[C:15]3[C:14]2=[O:23])[CH:9]1[S:24](Cl)=[O:25])[C:4]([O:6][CH3:7])=[O:5].FC(F)(F)C(O)=O>>[C:17]1(=[O:18])[N:13]([CH:10]2[C:11](=[O:12])[N:8]3[CH:3]([C:4]([O:6][CH3:7])=[O:5])[C:2](=[CH2:27])[CH2:1][S:24](=[O:25])[C@H:9]23)[C:14](=[O:23])[C:15]2=[CH:22][CH:21]=[CH:20][CH:19]=[C:16]12Participants
3
Procedure
A solution of 0.29 g. of methyl 3-methyl-2-(2-chlorosulfinyl-4-oxo-3-phthalimido-1-azetidinyl)-3-butenoate in 10 ml. of trifluoroacetic acid was refluxed for 30 minutes and then was evaporated in vacuo to dryness. The product was dissolved in 20 ml. of ethyl acetate. The resulting solution was washed successively with aqueous sodium bicarbonate (3X), water, and brine, dried (MgSO4), and evaporated in vacuo to dryness to provide methyl 7-phthalimido-3-methylenecepham-4-carboxylate 1-oxide.
Workup
- customwas evaporated in vacuo to dryness
- dissolutionThe product was dissolved in 20 ml
- washThe resulting solution was washed successively with aqueous sodium bicarbonate (3X), water, and brine
- dry with materialdried (MgSO4)
- customevaporated in vacuo to dryness
Sources & evidence
- ORD record
- ord-f5afdeffd71546fb968b32d40587eb58
- Source dataset
- uspto-grants-1977_10
- Patent number
- US04052387
Reaction notes
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