反応式
Cl.[Cl:2][C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[C:5]([O:11][CH2:12][CH3:13])[CH:4]=1.[CH2:14]([OH:16])[CH3:15]>>[ClH:2].[Cl:2][C:3]1[CH:10]=[CH:9][C:6]([C:7](=[NH:8])[O:16][CH2:14][CH3:15])=[C:5]([O:11][CH2:12][CH3:13])[CH:4]=1参加物
4
反応条件
- 温度
- 0 °C
実験手順
Hydrogen chloride gas was passed through a solution of 4-chloro-2-ethoxy-benzonitrile (670 mg, 3.689 mmol) in anhydrous ethanol (25 mL) cooled to 0° C. After 45 min, the hydrogen chloride gas was stopped and the reaction vessel was sealed with a Teflon stopper. It was stirred at room temperature for 5 d. The reaction vessel was cooled to 0° C. and the stopper was removed. The solvent was removed and the residue was triturated in diethyl ether to afford ethyl 4-chloro-2-ethoxy-benzimidate hydrochloride (913 mg, 94%). It was used without further purification.
後処理
- temperatureThe reaction vessel was cooled to 0° C.
- customthe stopper was removed
- customThe solvent was removed
- customthe residue was triturated in diethyl ether
出典と根拠
- ORDレコード
- ord-2d3b6a1461914dc486337f5e277cdc85
- 出典データセット
- uspto-grants-2003_09
- 特許番号
- US06617346B1
関連ノート
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