Acetic Acid → HCID 70593017, compound
Reaction equation
[NH:1]([CH2:8][C:9]1([CH3:35])[CH:13]([C:14]([O:16]CC(Cl)(Cl)Cl)=[O:15])[N:12]2[C:22](=[O:34])[CH:23]([NH:24][C:25](=[O:33])[CH2:26][C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[C@H:11]2[S:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O)(=O)C>CN(C)C=O.[Zn]>[NH:1]([CH2:8][C:9]1([CH3:35])[CH:13]([C:14]([OH:16])=[O:15])[N:12]2[C:22](=[O:34])[CH:23]([NH:24][C:25](=[O:33])[CH2:26][C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[C@H:11]2[S:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
2,2,2-Trichloroethyl 2-anilinomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate (1.00 g) was dissolved in dimethylformamide (5 ml). To this solution were added acetic acid (0.5 ml) and then zinc powder under cooling at -15° C. and the mixture was stirred for 6 hours. After the reaction, zinc powder was filtered off and the filtrate was poured into ethyl acetate. The solution was washed 4 times with water and dried over magnesium sulfate. After drying, the solvent was distilled off and the residue was dissolved in a small amount of methanol and then pulverized by adding water to the solution. The powder was collected by filtration, washed with water and dried to give 2-anilinomethyl-2-methyl-6-(2-phenylacetamido)-penam-3-carboxylic acid (0.50 g), mp. 120° C.
Workup
- filtrationwas filtered off
- additionthe filtrate was poured into ethyl acetate
- washThe solution was washed 4 times with water
- dry with materialdried over magnesium sulfate
- customAfter drying
- distillationthe solvent was distilled off
- dissolutionthe residue was dissolved in a small amount of methanol
- additionby adding water to the solution
- filtrationThe powder was collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-3dec5a1d54f74eaf877154819718a2f5
- Source dataset
- uspto-grants-1980_05
- Patent number
- US04203897
Reaction notes
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