3-Methyl-2-buten-1-OL → 3,3-Dimethylallylglycidyl ether

HRID 2256788

反応式

HRID 2256788 の反応式
[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

  1. stirringthe reaction mixture was stirred at room temperature for 24 hrs
  2. customTHF was removed on a rotary evaporator
  3. filtrationfiltered
  4. concentrationThe ether solution was concentrated on a rotary evaporator
  5. customthe brown oil obtained
  6. 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

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