Sodium Hydroxide → 4-[3-(1-Adamantyl)-4-methoxyphenylureido]benzoic acid

HRID 865887Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 865887
[OH-].[Na+].[C:3]12([C:13]3[CH:14]=[C:15]([NH:21][C:22](=[O:34])[NH:23][C:24]4[CH:33]=[CH:32][C:27]([C:28]([O:30]C)=[O:29])=[CH:26][CH:25]=4)[CH:16]=[CH:17][C:18]=3[O:19][CH3:20])[CH2:12][CH:7]3[CH2:8][CH:9]([CH2:11][CH:5]([CH2:6]3)[CH2:4]1)[CH2:10]2>CO>[C:3]12([C:13]3[CH:14]=[C:15]([NH:21][C:22](=[O:34])[NH:23][C:24]4[CH:33]=[CH:32][C:27]([C:28]([OH:30])=[O:29])=[CH:26][CH:25]=4)[CH:16]=[CH:17][C:18]=3[O:19][CH3:20])[CH2:10][CH:9]3[CH2:11][CH:5]([CH2:6][CH:7]([CH2:8]3)[CH2:12]1)[CH2:4]2

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 67714159Methyl 4-[3-(1-adamantyl)-4-methoxyphenylureido]benzoate

Produkt 1

HCID 677141384-[3-(1-Adamantyl)-4-methoxyphenylureido]benzoic acidAusbeute 87 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

6 g (0.15 mol) of sodium hydroxide are added to a solution of 6.08 g (14 mmol) of methyl 4-[3-(1-adamantyl)-4-methoxyphenylureido]benzoate in 75 of methanol and the mixture is stirred at room temperature for 3 hours and then heated to re flux for 3.5 hours. The reaction mixture is evaporated, the residue is then taken up with 100 ml of water and the mixture is acidified to pH 1. The solid is filtered off, rinsed with water, dried and recrystallized in a tetrahydrofuran/hexane mixture to yield 2.78 g (87%) of 4-[3-(1-adamantyl)-4-methoxyphenylureido]benzoic acid, melting point 279°-282° C.

Aufarbeitung

  1. temperatureheated
  2. customfor 3.5 hours
  3. customThe reaction mixture is evaporated
  4. filtrationThe solid is filtered off
  5. washrinsed with water
  6. customdried
  7. customrecrystallized in a tetrahydrofuran/hexane mixture

Quellen und Nachweise

ORD-Eintrag
ord-40c721b26c0d4cb9b3f99e28313eb91f
Quelldatensatz
uspto-grants-1996_10
Patentnummer
US05567721

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