(3,4-Dimethoxyphenyl)acetic acid → 2-(3,4-dimethoxyphenyl)-N-(beta-hydroxy-alpha,alpha-dimethylphenethyl)acetamide

HRID 443734ノート

反応式

HRID 443734 の反応式
[NH2:1][C:2]([CH:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[OH:6])([CH3:4])[CH3:3].[CH3:13][O:14][C:15]1[CH:16]=[C:17]([CH2:23][C:24](O)=[O:25])[CH:18]=[CH:19][C:20]=1[O:21][CH3:22].CCOC1N(C(OCC)=O)C2C(=CC=CC=2)C=C1.O1CCCC1CCO>>[CH3:13][O:14][C:15]1[CH:16]=[C:17]([CH2:23][C:24]([NH:1][C:2]([CH3:4])([CH3:3])[CH:5]([OH:6])[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[O:25])[CH:18]=[CH:19][C:20]=1[O:21][CH3:22]

参加物

5

実験手順

A solution of 8.3 g. (0.05 mole) of α-(1-amino-1-methylethyl)benzenemethanol, 9.8 g. (0.05 mole) of 3,4-dimethoxyphenylacetic acid and 13.6 g. (0.055 mole) of EEDQ (Aldrich Chem. Co.) in 300 ml. of tetrahydrofuran-ethanol is refluxed for 45 minutes and then allowed to stand for 20 hours at 25° C. The solution is evaporated in vacuo. The residue is taken up with 250 ml. of ethyl acetate, washed with dilute HCl, followed by washing with aqueous NaHCO3. Subsequently, the extract is washed with aqueous NaCl, dried (Na2SO4) and evaporated to dryness in vacuo. Crystallization of the residue from ether gives 14.0 g. (82% yield) of pure 2-(3,4-dimethoxyphenyl)-N-(β-hydroxy-α,α-dimethylphenethyl)acetamide, m.p. 123°-124° C.

後処理

  1. customThe solution is evaporated in vacuo
  2. washof ethyl acetate, washed with dilute HCl
  3. washby washing with aqueous NaHCO3
  4. washSubsequently, the extract is washed with aqueous NaCl
  5. dry with materialdried (Na2SO4)
  6. customevaporated to dryness in vacuo
  7. customCrystallization of the residue from ether
  8. customgives 14.0 g

出典と根拠

ORDレコード
ord-be27a9499e3c46a391df1b8fa8dbd5f3
出典データセット
uspto-grants-1981_04
特許番号
US04261890

反応ノート

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