反応式
Cl.[Br:2][C:3]1[CH:4]=[C:5]([NH:9][NH2:10])[CH:6]=[CH:7][CH:8]=1.[O:11]1[CH:15]=[CH:14][CH2:13][CH2:12]1>C1COCC1>[Br:2][C:3]1[CH:4]=[C:5]([NH:9][N:10]=[CH:15][CH2:14][CH2:13][CH2:12][OH:11])[CH:6]=[CH:7][CH:8]=1参加物
4
実験手順
Under anhydrous conditions a solution of 3-bromophenylhydrazine hydrochloride (22.5 g, 100 mmol) and 2,3-dihydrofuran (7.55 ml, 100 mmol) in 200 ml of dry THF was stirred at ambient temperature for 3 h. The reaction mixture was partitioned between EtOAc and H2O. The organic phase was washed with H2O and brine. After drying (Na2 SO4), the solvent was evaporated to give 25.6 g of the product as a brown oil. The product was of suitable purity for use in the next step.
後処理
- customThe reaction mixture was partitioned between EtOAc and H2O
- washThe organic phase was washed with H2O and brine
- customAfter drying (Na2 SO4)
- customthe solvent was evaporated
出典と根拠
- ORDレコード
- ord-71f44accceb34da08c5f8b2e174c5c94
- 出典データセット
- uspto-grants-1998_10
- 特許番号
- US05824699
関連ノート
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