反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[CH2:9][C:10]([OH:12])=O.S(Cl)([Cl:15])=O>>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[CH2:9][C:10]([Cl:15])=[O:12]参加物
3
実験手順
75.3 g (0.44 mol) of 2,6-difluorophenylacetic acid are dissolved in 96 ml (156.5 g; 1.32 mol) of thionyl chloride, stirred for 1 hour at 60° and then heated under reflux for 2 hours. The excess thionyl chloride is then distilled off and the residue is fractionated, yielding 79.5 g (95% of the theoretical yield) of 2,6-difluorophenylacetyl chloride.
後処理
- temperatureheated
- temperatureunder reflux for 2 hours
- distillationThe excess thionyl chloride is then distilled off
- customyielding 79.5 g (95% of the
出典と根拠
- ORDレコード
- ord-f2c7b09ca0e84b2f87402c200818a031
- 出典データセット
- uspto-grants-1992_03
- 特許番号
- US05098922
関連ノート
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