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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405778Generated: October 26, 2026

Allyl bromide → ((2-(Allyloxy)pent-4-enyloxy)methyl)benzene

https://huagongshe.com/reaction/405778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant1-(Benzyloxy)pent-4-en-2-olHCID 10035478—
SolventTetrahydrofuranHCID 8028—
Product((2-(Allyloxy)pent-4-enyloxy)methyl)benzeneHCID 12996273—

Reaction Steps

NaH (4.8 g, 120 mmol) was added portion wise to a stirred solution of 1-(benzyloxy)pent-4-en-2-ol (11) (15.3 g, 79.6 mmol) in THF (100 mL) at 0° C. After addition, the mixture was warmed to room temperature and stirred for another hour before it was cooled to 0° C. Allyl bromide (9 mL, 103.5 mmol) was added to the reaction and the resulting mixture was warmed to room temperature and then heated to 50° C. overnight. After cooling to room temperature, the mixture was quenched with saturated NH4Cl and worked up under standard conditions. The residue was purified over silica using Et2O and hexane to give ((2-(allyloxy)pent-4-enyloxy)methyl)benzene (12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754071B2
Source datasetuspto-grants-2014_06
ORD IDord-f9391ad3f9e24eab9ba4a508c82f6de1
Source noteuspto-grants-2014_06