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HRID 47169作成日:2026年10月25日

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

https://huagongshe.com/reaction/47169

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-2-buten-1-OLHCID 11173—
反応物EpibromohydrinHCID 18430—
反応物Sodium hydrideHCID 24758—
溶媒TetrahydrofuranHCID 8028—
生成物3,3-Dimethylallylglycidyl etherHCID 15580333—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699458B2
出典データセットuspto-grants-2004_03
ORD IDord-8a7ea803b1804dc29aa8ae7823c0926e
出典メモuspto-grants-2004_03