Ammonium Chloride → 5-Bromo-4-(2,4-difluorophenoxy)-2-methylbenzenamine
反応式
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[C:5]([CH3:11])=[CH:4][C:3]=1[O:12][C:13]1[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=1[F:20].[NH4+].[Cl-]>C1COCC1.CO.[Zn]>[Br:1][C:2]1[C:3]([O:12][C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=2[F:20])=[CH:4][C:5]([CH3:11])=[C:6]([NH2:8])[CH:7]=1参加物
実験手順
1-Bromo-2-(2,4-difluorophenoxy)-4-methyl-5-nitrobenzene (87.0 g, 253 mmol) was dissolved in THF (300 mL) and diluted with MeOH (900 mL). Zinc dust (82.7 g, 1.26 mol) was added and 1 L of saturated NH4Cl was added slowly so that the reaction temperature never exceeded 42° C. The reaction mixture was mechanically stirred vigorously for 16 hours, and the filtered through Celite and the filter cake was washed with ethyl acetate. The filtrate was then concentrated with 1.2 L of saturated NH4OAc. The THF/MeOH was removed and the solids were collected and washed with water. The solids were then stirred in 1 L water for 30 minutes, then collected via filtration and rinsed with water (1 L) in three portions. The resulting solid was dried under high vacuum for 48 hours to produce 64 g of the desired product (81% yield). MS (ESI+) m/z 314,316 (M+1, Br pattern) detected; 1H NMR (400 MHz, CDCl3) δ 6.92 (m, 1H), 6.91 (s, 1H), 6.75 (m, 2H), 6.70 (s, 1H), 3.57 (br. s, 2H), 2.08 (s, 3H).
後処理
- filtrationthe filtered through Celite
- washthe filter cake was washed with ethyl acetate
- concentrationThe filtrate was then concentrated with 1.2 L of saturated NH4OAc
- customThe THF/MeOH was removed
- customthe solids were collected
- washwashed with water
- stirringThe solids were then stirred in 1 L water for 30 minutes
- filtrationcollected via filtration
- washrinsed with water (1 L) in three portions
- customThe resulting solid was dried under high vacuum for 48 hours
出典と根拠
- ORDレコード
- ord-790e05a6b5ba4bae9485e712d88d4423
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08026233B2
反応ノート
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