Benzaldehyde → (S)-1-Benzyl-5-carboxy-2-pyrrolidinone
Reaction equation
Cl[C:2]1[C:7](C(F)(F)F)=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:12][NH:13][C:14](=[O:26])[C@@H:15]1[CH2:19][CH2:18][C:17](=[O:20])N1CC(C)(C)C.C(=[O:34])C1C=CC=CC=1>>[O:26]=[C:14]1[N:13]([CH2:12][C:3]2[CH:2]=[CH:7][CH:6]=[CH:5][CH:4]=2)[C@H:18]([C:17]([OH:20])=[O:34])[CH2:19][CH2:15]1Participants
3
Procedure
5-oxo-1-(phenylmethyl)proline was prepared in an analogous manner to that described above for the synthesis of 1-(2,2-dimethylpropyl)-5-oxoproline (example 100) but using benzaldehyde in the place of trimethylacetaldehyde.
Sources & evidence
- ORD record
- ord-38a887ced9484ef6b6f8654471eaf5ea
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08048907B2
Reaction notes
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