(3,4-Dimethoxyphenyl)acetic acid → 2-(3,4-dimethoxyphenyl)-N-(beta-hydroxy-alpha,alpha-dimethylphenethyl)acetamide
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
- customThe solution is evaporated in vacuo
- washof ethyl acetate, washed with dilute HCl
- washby washing with aqueous NaHCO3
- washSubsequently, the extract is washed with aqueous NaCl
- dry with materialdried (Na2SO4)
- customevaporated to dryness in vacuo
- customCrystallization of the residue from ether
- 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
読み込み中…