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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2393796생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/2393796

반응식

참여 물질

역할이름HCID투입량
반응물3-Methyl-2-buten-1-OLHCID 11173—
반응물EpibromohydrinHCID 18430—
반응물Sodium hydrideHCID 24758—
용매TetrahydrofuranHCID 8028—
생성물3,3-Dimethylallylglycidyl etherHCID 15580333—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05808091
출처 데이터셋uspto-grants-1998_09
ORD IDord-5d75156c546748ea99af4a4e39f19787
출처 메모uspto-grants-1998_09