HCID 13255323, compound → HCID 21326944, compound
Reaction equation
[CH2:1]([NH:17][C:18]1[CH:38]=[CH:37][C:21]([C:22]([O:24][CH:25]2[CH2:30][O:29]C(C3C=CC=CC=3)[O:27][CH2:26]2)=[O:23])=[CH:20][CH:19]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[H][H]>[Pd].C(O)(=O)C>[CH2:1]([NH:17][C:18]1[CH:19]=[CH:20][C:21]([C:22]([O:24][CH:25]([CH2:26][OH:27])[CH2:30][OH:29])=[O:23])=[CH:37][CH:38]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 2-phenyl-1,3-dioxan-5-yl 4-(n-hexadecylamino)benzoate, palladium black, and acetic acid is shaken under one atmosphere of hydrogen until hydrogen uptake ceases. The catalyst is separated by filtration and the solvent is evaporated. Crystallization from acetonitrile affords 1,3-dihydroxy-2-propyl 4-(n-hexadecylamino)benzoate as a white solid.
Workup
- customThe catalyst is separated by filtration
- customthe solvent is evaporated
- customCrystallization from acetonitrile
Sources & evidence
- ORD record
- ord-f5d659f5c83545b2812a2fda35d14e45
- Source dataset
- uspto-grants-1977_11
- Patent number
- US04058550
Reaction notes
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