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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779744Generated: October 25, 2026

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

https://huagongshe.com/reaction/1779744

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-2-buten-1-OLHCID 11173—
ReactantEpibromohydrinHCID 18430—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product3,3-Dimethylallylglycidyl etherHCID 15580333—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627286
Source datasetuspto-grants-1997_05
ORD IDord-25c92661dbef4bdeba198ec9a5fca83c
Source noteuspto-grants-1997_05