Hydrochloric Acid → HCID 18798338, compound
Reaction equation
[OH-:1].[Na+].[CH2:3](O)[CH3:4].C1(N=[C:13]([OH:75])[C:14]2[C:15](=[C:19]([O:55][C:56]3[CH:61]=[CH:60][C:59]([O:62][CH2:63][CH2:64][CH2:65][CH2:66][CH2:67][CH2:68]CCCCCC)=[CH:58][CH:57]=3)[C:20](=[C:24]([C:34]=2[O:35][C:36]2[CH:41]=[CH:40][C:39]([O:42][CH2:43][CH2:44][CH2:45][CH2:46]CCCCCCCC)=[CH:38][CH:37]=2)[C:25](=NC2C=CC=CC=2)[OH:26])[C:21]([OH:23])=[O:22])[C:16]([OH:18])=[O:17])C=CC=CC=1.Cl.[OH2:77]>>[CH2:43]([O:42][C:39]1[CH:38]=[CH:37][C:36]([O:35][C:34]2[C:14]([C:13]([OH:1])=[O:75])=[C:15]([C:16]([OH:18])=[O:17])[C:19]([O:55][C:56]3[CH:57]=[CH:58][C:59]([O:62][CH2:63][CH2:64][CH2:65][CH2:66][CH2:67][CH2:68][CH2:38][CH2:37][CH2:36][CH2:41][CH2:3][CH3:4])=[CH:60][CH:61]=3)=[C:20]([C:21]([OH:23])=[O:22])[C:24]=2[C:25]([OH:26])=[O:77])=[CH:41][CH:40]=1)[CH2:44][CH2:45][CH2:46][CH2:25][CH2:24][CH2:34][CH2:14][CH2:15][CH2:19][CH2:20][CH3:21]Participants
6
Procedure
Into 150 ml of 10% NaOH solution made from 1:1 (v:v) mixture of ethanol and water were dissolved 2 g of N,N'-diphenyl-3,6-bis[4-(n-dodecyloxy)phenyloxy]pyromellitic diimide obtained from above. This solution was refluxed for 72 hr under nitrogen atmosphere and then cooled to ambient temperature. When it was neutralized with 5% aqueous HCl, white precipitates were formed. These precipitates were filtered, air-dried and recrystallized from 1:1 (v:v) mixture of hexane and ethyl acetate to obtain 3,6-bis[4-(n-dodecyloxy)phenyloxy]pyromellitic acid.
Workup
- customobtained from above
- temperatureThis solution was refluxed for 72 hr under nitrogen atmosphere
- customwhite precipitates
- customwere formed
- filtrationThese precipitates were filtered
- customair-dried
- customrecrystallized from 1:1 (v:v) mixture of hexane and ethyl acetate
Sources & evidence
- ORD record
- ord-dcb247348ae5496db88ecf4f3a4d5f5e
- Source dataset
- uspto-grants-2000_04
- Patent number
- US06046342
Reaction notes
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