Sodium Hydroxide → 22-(2-Hydroxy-3,4-dimethoxy-6-methylphenyl)docosanoic acid

HRID 2412846Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2412846
[OH:1][C:2]1[C:7]([O:8][CH3:9])=[C:6]([O:10][CH3:11])[CH:5]=[C:4]([CH3:12])[C:3]=1[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][C:34]([O:36]C)=[O:35].[OH-].[Na+]>CO>[OH:1][C:2]1[C:7]([O:8][CH3:9])=[C:6]([O:10][CH3:11])[CH:5]=[C:4]([CH3:12])[C:3]=1[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][C:34]([OH:36])=[O:35]

Komponenten

4

Versuchsvorschrift

In 15 ml of methanol is dissolved 300 mg of methyl 22-(2-hydroxy-3,4-dimethoxy-6-methylphenyl)docosanoate followed by addition of 20 ml of a 14% aqueous solution of sodium hydroxide. The mixture is stirred at 50°-60° C. for 1.5 hours. The reaction mixture is made acidic with 3N--HCl and extracted with ethyl acetate. The extract is washed with water and, after drying, the solvent is distilled off under reduced pressure. The residue is recrystallized from methanol to obtain 22-(2-hydroxy-3,4-dimethoxy-6-methylphenyl)docosanoic acid (IV:n=21), m.p. 67° C.-68° C. NMR(δ, in deuteriochloroform): 1.27(38H,b,CH2), 2.24(3H,s,nuclear CH3), 2.28-2.56(4H,m,CH2COO, nuclear CH2), 3.80(3H,s,OCH3), 3.84(3H,s,OCH3), 6.24(1H,s, nuclear H)

Aufarbeitung

  1. extractionHCl and extracted with ethyl acetate
  2. washThe extract is washed with water
  3. customafter drying
  4. distillationthe solvent is distilled off under reduced pressure
  5. customThe residue is recrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-9fdae08b440143c3ab3bdc4481e978e2
Quelldatensatz
uspto-grants-1985_01
Patentnummer
US04495104

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