反応式
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH2:3][CH2:2]1.[CH2:8]([OH:14])[CH2:9]/[CH:10]=[CH:11]\[CH2:12][CH3:13].N1C=CC=CC=1.Cl>ClCCl.CN(C1C=CC=CN=1)C.CCOCC>[CH2:8]([O:14][C:4](=[O:5])[CH2:3][CH2:2][C:1]([OH:6])=[O:7])[CH2:9][CH:10]=[CH:11][CH2:12][CH3:13]参加物
8
実験手順
A mixture of 100 g succinic anhydride, 100 g cis-3-hexen-1-ol, 88.5 ml pyridine and 7.3 g dimethylaminopyridine in 500 ml dichloromethane was refluxed for 4 hours. Ether was added and the mixture was acidified with HCl 2N then washed with brine. The organic layer was dried over magnesium sulfate and concentrated. The residue was distilled under vacuum to afford 185 g of product.
後処理
- temperaturewas refluxed for 4 hours
- washthen washed with brine
- dry with materialThe organic layer was dried over magnesium sulfate
- concentrationconcentrated
- distillationThe residue was distilled under vacuum
出典と根拠
- ORDレコード
- ord-e3e39f96d5b94d9e846a89f493a7d16f
- 出典データセット
- uspto-grants-2002_08
- 特許番号
- US06437150B1
関連ノート
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