反応式
C(N(CC)CC)C.[CH3:8][O:9][C:10]1[CH:11]=[C:12]([CH:18]=[C:19]([O:23][CH3:24])[C:20]=1[O:21][CH3:22])[CH:13]=[CH:14][C:15](O)=[O:16].ClC(OCC)=O.Cl.[CH3:32][NH:33][OH:34].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CN(C)C=O>[CH3:8][O:9][C:10]1[CH:11]=[C:12]([CH:18]=[C:19]([O:23][CH3:24])[C:20]=1[O:21][CH3:22])[CH:13]=[CH:14][C:15]([N:33]([CH3:32])[OH:34])=[O:16]参加物
反応条件
- 温度
- -12 °C
実験手順
Triethylamine (3.07 ml, 22 mmol) was added to a stirred solution of 3,4,5-trimethoxycinnamic acid (4.76 g, 20 mmol) in N,N-dimethylformamide (30 ml). The resulting solution was cooled to -12° C., and ethyl chloroformate (2.00 ml, 21 mmol) was added dropwise with stirring. After 15 minutes, solid N-methylhydroxylamine hydrochloride (1.84 g, 22 mmol) was added, followed by triethylamine (3.2 ml, 23 mmol). The mixture was allowed to warm to room temperature, stirred overnight, and poured into 150 ml of 1% aqueous citric acid. The mixture was extracted twice with ethyl ether, and the combined extracts washed successively with water and brine, then dried over MgSO4, filtered, and evaporated. The residue was recrystallized from ethyl acetate to provide 1.82 g (34% yield) of the titled compound as colorless crystals, mp 169°-170° C.
後処理
- temperatureto warm to room temperature
- stirringstirred overnight
- extractionThe mixture was extracted twice with ethyl ether
- washthe combined extracts washed successively with water and brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated
- customThe residue was recrystallized from ethyl acetate
出典と根拠
- ORDレコード
- ord-3701ffc56a7f42ecb653d82459bf55ba
- 出典データセット
- uspto-grants-1989_04
- 特許番号
- US04820828
関連ノート
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