Hydrochloric Acid → HCID 18798334, compound
Reaction equation
[OH-:1].[Na+].C(O)C.C1(N=[C:13]([OH:59])[C:14]2[C:15](=[C:19]([O:47][C:48]3[CH:53]=[CH:52][C:51]([O:54][CH2:55][CH2:56][CH2:57][CH3:58])=[CH:50][CH:49]=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][CH3:46])=[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.[OH2:61]>>[CH2:43]([O:42][C:39]1[CH:40]=[CH:41][C:36]([O:35][C:34]2[C:24]([C:25]([OH:1])=[O:26])=[C:20]([C:21]([OH:23])=[O:22])[C:19]([O:47][C:48]3[CH:53]=[CH:52][C:51]([O:54][CH2:55][CH2:56][CH2:57][CH3:58])=[CH:50][CH:49]=3)=[C:15]([C:16]([OH:18])=[O:17])[C:14]=2[C:13]([OH:59])=[O:61])=[CH:37][CH:38]=1)[CH2:44][CH2:45][CH3:46]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-butyloxy)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-butyloxy)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-1e5c421c65b34895af67245f8d0318b5
- Source dataset
- uspto-grants-2000_04
- Patent number
- US06046342
Reaction notes
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