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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methyl-2-buten-1-OL | HCID 11173 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,3-Dimethylallylglycidyl ether | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05627286 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-25c92661dbef4bdeba198ec9a5fca83c |
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| Source note | uspto-grants-1997_05 |
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