Hydrochloric Acid → 4-Hydrazinyl-2-(methoxymethyl)benzonitrile hydrochloride
反応式
F[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([CH2:10][O:11][CH3:12])[CH:3]=1.O.[NH2:14][NH2:15].C(O)C.[ClH:19]>CO.C(OCC)C>[ClH:19].[NH:14]([C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([CH2:10][O:11][CH3:12])[CH:3]=1)[NH2:15]参加物
7
実験手順
A mixture of 4-fluoro-2-(methoxymethyl)benzonitrile (110 mg, 0.67 mmol), hydrazine monohydrate (133 mg, 0.13 mL, 2.6 mmol) and ethanol (5 mL) was heated to reflux overnight. The mixture was cooled to room temp and condensed. The residue was dissolved in methanol and treated with 2.0 N Hydrogen chloride in diethyl ether. The solvent was removed and the solid was dried to give 4-hydrazinyl-2-(methoxymethyl)benzonitrile hydrochloride as an off-white solid.
後処理
- temperaturewas heated
- temperatureto reflux overnight
- customcondensed
- customThe solvent was removed
- customthe solid was dried
出典と根拠
- ORDレコード
- ord-6b1498ae6dcc4bf6858cdda7915a81dd
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07781428B2
反応ノート
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