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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464692Generated: October 30, 2026

Allyl bromide → 3-Allyloxy-4-bromoanisol

https://huagongshe.com/reaction/1464692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-methoxyphenolHCID 13493839—
SolventAcetonitrileHCID 6342—
Product3-Allyloxy-4-bromoanisolHCID 14703422111%

Reaction Steps

To a solution of 4-bromo-3-hydroxyanisol (14.49, 59.3 mmol), synthesized by known methods, in CH3CN (200 ml), dry potassium carbonate (20 g) and allylbromide (8.0 ml, 92.4 mmol) was added. The reaction mixture was stirred and refluxed for 1 hour and thereafter cooled to room temperature, filtered and evaporated. The residue was dissolved in ether and extracted with water. The organic layer was separated and dried (Na2SO4). Evaporation of the solvent afforded 16.0 g (93%) of 3-allyloxy-4-bromoanisol as an oil. GC/MS (HP-5970A) m/e=244 (40) M+ and M+ -1 at m/e=242 (40), 163 (100), 149 (97), 135 (62).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05306830
Source datasetuspto-grants-1994_04
ORD IDord-b51aa913910342a8b842f3b306dd0416
Source noteuspto-grants-1994_04