反応式
[Br:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[CH:6][C:7]=1[F:8].[CH2:10](Br)[CH:11]=[CH2:12].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH2:12]([O:9][C:4]1[CH:5]=[CH:6][C:7]([F:8])=[C:2]([Br:1])[CH:3]=1)[CH:11]=[CH2:10]参加物
5
実験手順
A mixture of 0.65 gm (3.43 mMol) 3-bromo-4-fluorophenol, 0.60 mL (6.86 mMol) allyl bromide, and 0.71 gm (5.15 mMol) potassium carbonate in 6 mL acetone was stirred at reflux for 13 hours. The reaction mixture was concentrated under reduced pressure and the residue subjected to silica gel chromatography, eluting with hexane. Fractions containing product were combined and concentrated under reduced pressure to provide 61% of the desired compound.
後処理
- temperatureat reflux for 13 hours
- concentrationThe reaction mixture was concentrated under reduced pressure
- washeluting with hexane
- additionFractions containing product
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-9f1bda2d7be54cefa7131823b99501cf
- 出典データセット
- uspto-grants-2006_05
- 特許番号
- US07045545B1
関連ノート
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