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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045402Generated: October 27, 2026

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

https://huagongshe.com/reaction/1045402

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 numberUS08569283B2
Source datasetuspto-grants-2013_10
ORD IDord-04e899cb62dd442ca75e4bdf08a97004
Source noteuspto-grants-2013_10