HCID 22269456, compound → HCID 22269455, compound

HRID 488957Notes

Reaction equation

HRID 488957 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

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 catalyst) 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

  1. filtrationThe reaction mixture was filtered through Celite™ diatomaceous earth
  2. filtrationfilter agent
  3. customto remove the catalyst
  4. concentrationThe filtrate was concentrated in vacuo

Sources & evidence

ORD record
ord-3650f16d5fb1443faa91940713c43b10
Source dataset
uspto-grants-2005_12
Patent number
US06974877B2

Reaction notes

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