反応式
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([I:12])[C:3]=1N.Cl.N([O-])=O.[Na+].[PH2](O)=O>O>[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:9])([F:10])[F:11])[CH:5]=[C:4]([I:12])[CH:3]=1参加物
反応条件
- 温度
- 57.5 °C
実験手順
2-Chloro-6-iodo-4-(trifluoromethyl)benzenamine (i.e. the product of Example 4) (31.8 g, 98.9 mmol) was added to hydrochloric acid (36%, 190 mL) and the mixture was warmed to 55-60° C. for 20 min. The mixture was cooled to 0° C. Sodium nitrite (13.6 g, 197 mmol) in water (36 mL) was added over 30 min. When the addition was complete the mixture was stirred at 0-5° C. for 70 min. Hypophosphorous acid (50%, 36.5 mL, 351 mmol) was added dropwise at 5-10° C. over 40 min. When the addition was complete the mixture spontaneously warmed briefly to 35° C., and was then cooled to 10-20° C. After stirring at 10-20° C. for 2 h, the mixture was stored in a refrigerator overnight. Then the mixture was warmed to room temperature and was stirred for 1 h. The mixture was diluted with water (400 mL) and extracted with ether (2×250 mL). The combined extracts were dried and evaporated. Distillation gave the product as an oil (19.93 g, 66% yield), b.p. 98-112° C. at 2.0 kPa.
後処理
- temperatureThe mixture was cooled to 0° C
- additionWhen the addition
- additionWhen the addition
- temperaturespontaneously warmed briefly to 35° C.
- temperaturewas then cooled to 10-20° C
- stirringAfter stirring at 10-20° C. for 2 h
- customwas stored in a refrigerator overnight
- temperatureThen the mixture was warmed to room temperature
- stirringwas stirred for 1 h
- extractionextracted with ether (2×250 mL)
- customThe combined extracts were dried
- customevaporated
- distillationDistillation
出典と根拠
- ORDレコード
- ord-01f05c5312f5411fb66a6b77cf8c2465
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08546618B2
関連ノート
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