Sodium Hydroxide → 1,4-Bis[(phenylmethyl)oxy]-2,3-naphthalenedicarboxylic acid

HRID 222423Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 222423
[C:1]1([CH2:7][O:8][C:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:12]([O:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[C:11]([C:27]([O:29]CC)=[O:28])[C:10]=2[C:32]([O:34]CC)=[O:33])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>C(O)C>[C:1]1([CH2:7][O:8][C:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:12]([O:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[C:11]([C:27]([OH:29])=[O:28])[C:10]=2[C:32]([OH:34])=[O:33])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Komponenten

4

Versuchsvorschrift

A mixture of diethyl 1,4-bis[(phenylmethyl)oxy]-2,3-naphthalenedicarboxylate (4.78 g, 9.88 mmol), ethanol (75 ml), and 2N aqueous sodium hydroxide solution (75 ml) was refluxed for 2 hours. The reaction mixture was cooled and evaporated. This was acidified with HCl (2N) and the resulting cream solid was collected by filtration and washed with water. This was dried under vacuum to give the title compound (3.79 g, 8.86 mmol). LC/MS: Rt=3.15, [MH]− 427.

Aufarbeitung

  1. temperaturewas refluxed for 2 hours
  2. temperatureThe reaction mixture was cooled
  3. customevaporated
  4. filtrationthe resulting cream solid was collected by filtration
  5. washwashed with water
  6. customThis was dried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-bc686003fcb94a83bb38f789ec6cb61c
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08207213B2

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