Sodium Hydroxide → 1-Amino-5-fluoronaphthalene
反応式
[F:1][C:2]1[C:11]2[C:6](=[C:7]([N+:12]([O-])=O)[CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>CCO.[Fe]>[NH2:12][C:7]1[C:6]2[C:11](=[C:2]([F:1])[CH:3]=[CH:4][CH:5]=2)[CH:10]=[CH:9][CH:8]=1参加物
5
実験手順
A solution of compound 208A (62 mg, 0.32 mmol) in 1 mL EtOH containing 0.1 mL 12 N HCl was heated to reflux. Iron powder (62 mg, 1.11 mmol) was added in small portions and heating was continued for 2 h. The mixture was cooled, neutralized with 1 N NaOH solution and the aqueous layer was extracted with CH2Cl2. The combined organic phases were dried over MgSO4 and concentrated in vaccuo to leave a residue which was purified by flash chromatography on silica gel eluting with 40 to 80% EtOAc in hexanes to give 42 mg (0.26 mmol, 80%) of compound 208B as a yellow solid.
後処理
- temperatureheating
- temperatureThe mixture was cooled
- extractionthe aqueous layer was extracted with CH2Cl2
- dry with materialThe combined organic phases were dried over MgSO4
- concentrationconcentrated in vaccuo
- customto leave a residue which
- customwas purified by flash chromatography on silica gel eluting with 40 to 80% EtOAc in hexanes
出典と根拠
- ORDレコード
- ord-fc53b40d70074079ab4bc3bd9c813de8
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07141578B2
反応ノート
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