反応式
[Br:1][C:2]([F:10])([F:9])[C:3]([Cl:8])([F:7])[CH2:4][CH2:5]Br.CN1CCCC1=[O:17]>O>[Br:1][C:2]([F:10])([F:9])[C:3]([Cl:8])([F:7])[CH2:4][CH2:5][OH:17]参加物
4
反応条件
- 温度
- 130 °C
実験手順
A mixture of 1,4-dibromo-2-chloro-1,1,2-trifluorobutane (XVI) (7.5 g, 24.6 mmol), 1-methyl-2-pyrrolidinone (14 mL) and water (2.5 mL) was heated at 130° C. for 16 hours. The mixture was cooled to room temperature, diluted with water (80 mL) and extracted with ether (2×75 mL). The ether extract was washed with water (3×40 mL,), brine, and dried over anhydrous magnesium sulfate. The residue obtained after evaporation of the solvent was chromatographed over silica gel to give 2.9 g (49%) of the desired alcohol as a clear off.
後処理
- temperatureThe mixture was cooled to room temperature
- extractionextracted with ether (2×75 mL)
- extractionThe ether extract
- washwas washed with water (3×40 mL,), brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe residue obtained
- customafter evaporation of the solvent
- customwas chromatographed over silica gel
出典と根拠
- ORDレコード
- ord-5c7a55070fa145c29310d05548ac7fed
- 出典データセット
- uspto-grants-1997_05
- 特許番号
- US05627174
関連ノート
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