HCID 54487808, compound → HCID 54390892, compound
Reaction equation
[CH3:1][N:2]1[C:5](=[O:6])[CH2:4][C@H:3]1[C:7]([O:9]CC1C=CC=CC=1)=[O:8].[H][H]>CO.[Pd]>[CH3:1][N:2]1[C:5](=[O:6])[CH2:4][C@H:3]1[C:7]([OH:9])=[O:8]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
In 10 ml of methanol was dissolved 450 mg of compound (11) and 45 mg of 10% Pd-C was added to the solution followed by catalytic hydrogenation at ambient temperature under an atmospheric pressure of hydrogen. The catalyst was filtered off and the solvent was removed by distillation under reduced pressure to obtain 258 mg of (S)-1-methyl-4-oxo-2-azetidinecarboxylic acid (12).
Workup
- additionwas added to the solution
- filtrationThe catalyst was filtered off
- customthe solvent was removed by distillation under reduced pressure
Sources & evidence
- ORD record
- ord-d486b7cdbee54fd58211f266dc427ea4
- Source dataset
- uspto-grants-1988_01
- Patent number
- US04719207
Reaction notes
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