2-[[(Ethoxy)(phthalimidomethyl)phosphinyl]methyl]-4-methylvalerate → 2-[[(Ethoxy)(phthalimidomethyl)phosphinyl]methyl]-4-methylvaleric acid
Reaction equation
[CH2:1]([O:3][P:4]([CH2:18][CH:19]([CH2:23][CH:24]([CH3:26])[CH3:25])[C:20]([O-:22])=[O:21])([CH2:6][N:7]1[C:11](=[O:12])[C:10]2=[CH:13][CH:14]=[CH:15][CH:16]=[C:9]2[C:8]1=[O:17])=[O:5])[CH3:2]>C(O)C.[Pd]>[CH2:1]([O:3][P:4]([CH2:18][CH:19]([CH2:23][CH:24]([CH3:25])[CH3:26])[C:20]([OH:22])=[O:21])([CH2:6][N:7]1[C:8](=[O:17])[C:9]2=[CH:16][CH:15]=[CH:14][CH:13]=[C:10]2[C:11]1=[O:12])=[O:5])[CH3:2]Participants
4
Procedure
4.5 g of benzyl (R or S)-2-[[(ethoxy)(phthalimidomethyl)phosphinyl]methyl]-4-methylvalerate were dissolved in 120 ml of ethanol and the solution was hydrogenated over 1.6 g of 10% palladium-on-charcoal for 5.5 hours. After filtration and evaporation of the filtrate, there were obtained 3.0 g of (R or S)-2-[[(ethoxy)(phthalimidomethyl)phosphinyl]methyl]-4-methylvaleric acid in the form of A white foam.
Workup
- filtrationAfter filtration and evaporation of the filtrate
Sources & evidence
- ORD record
- ord-04ed2ed3a02e46a68151d8cf3701f54d
- Source dataset
- uspto-grants-1989_12
- Patent number
- US04885283
Reaction notes
Loading…