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

HRID 2412846ノート

反応式

HRID 2412846 の反応式
[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]

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 12824096HCID 12824096、化合物

生成物 1

HCID 1282407422-(2-Hydroxy-3,4-dimethoxy-6-methylphenyl)docosanoic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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)

後処理

  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

出典と根拠

ORDレコード
ord-9fdae08b440143c3ab3bdc4481e978e2
出典データセット
uspto-grants-1985_01
特許番号
US04495104

反応ノート

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