HCID 22269456, compound → HCID 22269455, compound
Reaction equation
[CH2:1]([C:10]1[CH:46]=[CH:45][C:13]([C:14]([C:16]2[CH:24]=[C:23]([C:25]([OH:27])=[O:26])[C:22]([C:28](=O)[C:29]3[CH:34]=[CH:33][C:32]([CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])=[CH:31][CH:30]=3)=[CH:21][C:17]=2[C:18]([OH:20])=[O:19])=O)=[CH:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[H][H]>[Pd].O1CCCC1>[CH2:1]([C:10]1[CH:46]=[CH:45][C:13]([CH2:14][C:16]2[CH:24]=[C:23]([C:25]([OH:27])=[O:26])[C:22]([CH2:28][C:29]3[CH:30]=[CH:31][C:32]([CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])=[CH:33][CH:34]=3)=[CH:21][C:17]=2[C:18]([OH:20])=[O:19])=[CH:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 109 grams of 2,5-bis(4-nonylbenzoyl)terephthalic acid 1500 mL of tetrahydrofuran, and 7.43 grams of 10% palladium on carbon (as a catayst)was heated at 65° C. for 17 hours in an atmosphere of hydrogen at 270 kPa. The reaction mixture was filtered through Celite™ diatomaceous earth filter agent to remove the catalyst. The filtrate was concentrated in vacuo to give 2,5-bis(4-nonylbenzyl)terephthalic acid.
Workup
- filtrationThe reaction mixture was filtered through Celite™ diatomaceous earth
- filtrationfilter agent
- customto remove the catalyst
- concentrationThe filtrate was concentrated in vacuo
Sources & evidence
- ORD record
- ord-f606a81ca956492fb1159b61381853c5
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06864396B2
Reaction notes
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