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HRID 1779744作成日:2026年10月26日

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

https://huagongshe.com/reaction/1779744

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 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. bp: 93°-94° C./10 mm. Yield: 17.2 g (60.5%). 1H NMR (CDCl3) ε 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05627286
出典データセットuspto-grants-1997_05
ORD IDord-25c92661dbef4bdeba198ec9a5fca83c
出典メモuspto-grants-1997_05