Hydrochloric Acid → HCID 18798334, compound

HRID 1003801Notes

Reaction equation

HRID 1003801 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

  1. customobtained from above
  2. temperatureThis solution was refluxed for 72 hr under nitrogen atmosphere
  3. customwhite precipitates
  4. customwere formed
  5. filtrationThese precipitates were filtered
  6. customair-dried
  7. 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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