تفاعل #75447

ord-8a7ea803b1804dc29aa8ae7823c0926e

معادلة التفاعل

BrCC1CO1
Epibromohydrin
CC(C)=CCO
dimethylallyl alcohol
[H-].[Na+]
sodium hydride
CC(C)=CCOCC1CO1
title product
CC(C)=CCOCC1CO1
3,3-Dimethylallylglycidyl Ether

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred at room temperature for 24 hours
  2. 2
    أخرىTHF was removed on a rotary evaporator
  3. 3
    ترشيحfiltered
  4. 4
    تركيزThe ether solution was concentrated on a rotary evaporator
  5. 5
    أخرىthe brown oil obtained
  6. 6
    workup.DISTILLATIONwas distilled under vacuum

الإجراء التجريبي

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) δ1.68 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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06699458B2uspto-grants-2004_03