HCID 54054639, compound → HCID 53835619, compound
Reaction equation
[CH2:1]([O:15][C:16]([C:18]1[CH:23]=[C:22]([N+:24]([O-])=O)[CH:21]=[C:20]([C:27]([O:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])=[O:28])[CH:19]=1)=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]>[Pd].C(OCC)(=O)C.C1COCC1>[CH2:30]([O:29][C:27]([C:20]1[CH:21]=[C:22]([NH2:24])[CH:23]=[C:18]([C:16]([O:15][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])=[O:17])[CH:19]=1)=[O:28])[CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43]Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
A mixture of 2.09 g of 5-nitro-1,3-benzenedicarboxylic acid ditetradecyl ester and 0.5 g of 10% palladium on carbon in 80 ml of ethyl acetate and 25 ml of THF was shaken under an initial hydrogen pressure of 53 psi for 17 hours. The catalyst was removed by filtration and the filtrate was concentrated to give 1.96 g of pure 5-amino-1,3-benzenedicarboxylic acid ditetradecyl ester, mp 74°-75°.
Workup
- customThe catalyst was removed by filtration
- concentrationthe filtrate was concentrated
Sources & evidence
- ORD record
- ord-fd281d2b59bc4f3f86392a63bfc253b7
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05446189
Reaction notes
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