反応式
[CH2:1]([O:8][C:9]1[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=1[CH:11]=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:17]([Mg]Br)=[CH2:18]>C1COCC1>[CH2:1]([O:8][C:9]1[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=1[CH:11]([OH:12])[CH:17]=[CH2:18])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
2-(benzyloxy)benzaldehyde (5g, 23.6 mmol) was reacted with vinylmagnesium bromide in THF (90 ml) at 0 C. The reaction was quenched with 2 N HCl and the product was extracted in i-PrOAc, dried over Na2SO4 and purified by flash chromatography with EtOAc:toluene 2.5:97.5.
後処理
- customThe reaction was quenched with 2 N HCl
- extractionthe product was extracted in i-PrOAc
- dry with materialdried over Na2SO4
- custompurified by flash chromatography with EtOAc:toluene 2.5:97.5
出典と根拠
- ORDレコード
- ord-a4708b1709d247f8a0d9098dd75df039
- 出典データセット
- uspto-grants-2001_04
- 特許番号
- US06211197B1
関連ノート
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