反応式
[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][OH:5].[H-].[Na+].[CH2:9]([CH:11]1[O:13][CH2:12]1)Br>O1CCCC1>[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][O:5][CH2:9][CH:11]1[O:13][CH2:12]1参加物
5
実験手順
To a solution of 3,3-dimethylallyl alcohol (17.3 g, 20.5 mL, 0.2 mol) in dry tetrahydrofuran (THF) (200 mL) was added sodium hydride (4.8 g, 0.2 mol) in portions and the mixture was stirred at room temperature for 1 hr. Epibromohydrin (27.4 g, 17.12 mL, 0.2 mol) was added dropwise and the reaction mixture was stirred at room temperature for 24 hrs. THF was removed on a rotary evaporator and the residue was taken up in ether and filtered. The ether solution was concentrated on a rotary evaporator and the brown oil obtained was distilled under vacuum.
後処理
- stirringthe reaction mixture was stirred at room temperature for 24 hrs
- customTHF was removed on a rotary evaporator
- filtrationfiltered
- concentrationThe ether solution was concentrated on a rotary evaporator
- customthe brown oil obtained
- distillationwas distilled under vacuum
出典と根拠
- ORDレコード
- ord-85453916f8e0490a9eb28b355a5f45c6
- 出典データセット
- uspto-grants-1997_08
- 特許番号
- US05656254
関連ノート
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