反応式
[CH3:1][C:2]1(O)[CH:9]2[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:11][CH:3]1[CH2:4]3)[CH2:8]2.[C:13](Cl)(=[O:16])[CH:14]=[CH2:15].C([O:20]CC)C>>[C:13]([O:16][C:3]12[CH2:11][CH:7]3[CH2:6][CH:5]([CH2:10][CH:9]([CH2:8]3)[CH:2]1[CH3:1])[CH2:4]2)(=[O:20])[CH:14]=[CH2:15]参加物
4
実験手順
200 mL of diethyl ether was put into a round-neck flask, 41.5 g of 2-methyl-2-adamantanol and 27.6 g of tetraethyl amine were added thereto and then 22.6 g of acryloyl chloride was dropped. The reactant was reacted at room temperature for about 12 hours and then filtered using diethyl ether. Subsequently, the solvent was removed by an evaporator and then the reactant product was obtained using vacuum distillation (yield: 55%).
後処理
- customThe reactant was reacted at room temperature for about 12 hours
- filtrationfiltered
- customSubsequently, the solvent was removed by an evaporator
- customthe reactant product was obtained
- distillationvacuum distillation (yield: 55%)
出典と根拠
- ORDレコード
- ord-36f2de1457284bf3b0fda06e472eab7b
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07084227B2
関連ノート
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