反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11]O.S(Cl)([Cl:15])=O>C1(C)C=CC=CC=1.ClCCl>[Cl:15][CH2:11][C:2]1[CH:3]=[CH:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH:1]=1参加物
5
実験手順
To 1.26 mol of naphth-2-yl-methanol in 1.5 liters of toluene there are slowly added 3.8 mol of thionyl chloride. The mixture is then heated at reflux for two hours. After cooling, the solvent is evaporated off. The crude product is taken up in toluene twice and evaporated. The oil obtained is taken up in dichloromethane, washed and dried. After filtering and evaporating, the oil obtained is distilled to yield the expected product.
後処理
- temperatureThe mixture is then heated
- temperatureat reflux for two hours
- temperatureAfter cooling
- customthe solvent is evaporated off
- customevaporated
- customThe oil obtained
- washwashed
- customdried
- filtrationAfter filtering
- customevaporating
- customthe oil obtained
- distillationis distilled
出典と根拠
- ORDレコード
- ord-2b76a36fe9d8421e9983fe191e681c45
- 出典データセット
- uspto-grants-2004_06
- 特許番号
- US06747032B2
関連ノート
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