HCID 22561366, compound → HCID 22269445, compound
Reaction equation
[CH3:1][C:2]1[CH:30]=[CH:29][C:5]([C:6]([C:8]2[CH:16]=[C:15]([C:17](=O)[C:18]3[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=3)[C:11]([C:12]([OH:14])=[O:13])=[CH:10][C:9]=2[C:26]([OH:28])=[O:27])=O)=[CH:4][CH:3]=1.[H][H]>[Pd].C(O)(=O)C>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][C:8]2[CH:16]=[C:15]([CH2:17][C:18]3[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=3)[C:11]([C:12]([OH:14])=[O:13])=[CH:10][C:9]=2[C:26]([OH:28])=[O:27])=[CH:29][CH:30]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 21.1 grams of 4,6-bis(4-methylbenzoyl)isophthalic acid, 350 mL of acetic acid, and 2.10 grams of 5% palladium on carbon (as a catalyst) was heated to 65° C. for 17 hours in an atmosphere of hydrogen at 270 kPa. The resulting mixture was filtered through Celite™ diatomaceous earth filter agent to remove the catalyst. The filtrate was concentrated in vacuo to give 4,6-bis(4-methylbenzyl)isophthalic acid.
Workup
- filtrationThe resulting mixture was filtered through Celite™ diatomaceous earth
- filtrationfilter agent
- customto remove the catalyst
- concentrationThe filtrate was concentrated in vacuo
Sources & evidence
- ORD record
- ord-8b20d8a3588847598aafb79c19749a54
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06864396B2
Reaction notes
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