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

HRID 2293903

반응식

HRID 2293903 반응식
[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>C1COCC1>[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][O:5][CH2:9][CH:11]1[O:13][CH2:12]1

참가 물질

5

실험 절차

To a solution of dimethylallyl alcohol (17.3 g, 20.5 mL, 0.2 mol) in dry THF (200 mL), sodium hydride (4.8 g, 0.2 mol) was added in portions and the mixture was stirred at room temperature for 1 hour. Epibromohydrin (27.4 g, 17.12 mL, 0.2 mol) was added to this reaction mixture dropwise and the mixture was stirred at room temperature for 24 hours. 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 to yield the title product. bp. 93°-94° C./10 mm. Yield: 17.2 g (60.5%). 1H NMR (CDCl3) δ 1.68 and 1.75 (s, 6H, CH3), 2.61 and 2.88 (dd, 2H, oxirane CH2), 3.17 (m, 1H, oxirane CH), 3.38 and 3.7 (m, 2H, CH2OCH2CH), 4.05 (m, 2H, CH2OCH2CH), 5.35 (m, 1H, >C=CH).

후처리

  1. stirringthe mixture was stirred at room temperature for 24 hours
  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

출처 및 근거

ORD 기록
ord-5707fc1dbc224fb1a0be0b9455aef82a
출처 데이터셋
uspto-grants-1997_11
특허 번호
US05688487

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