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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381578Generated: November 4, 2026

Allyl bromide → HCID 28562283, compound

https://huagongshe.com/reaction/2381578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Hydroxy-4-methoxybenzyl alcoholHCID 78089—
SolventAcetonitrileHCID 6342—
ProductHCID 28562283HCID 2856228399.5%

Reaction Steps

A mixture of 3-hydroxy-4-methoxybenzylalcohol (0.80 g, 7.79 mmol.), allyl bromide (0.45 ml, 5.9 mmol.), acetonitrile (20 ml), and potassium carbonate (1.08 g, 7.8 mmol.) was reluxed for 18 hours, then concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with water and brine. The organic layer was dried (MgSO4) and evaporated to give the product as a yellow oil (1.14 g, 57%). 1H NMR (300 MHz, CDCl3) δ 1.90 (s, 1H), 3.79 (s, 3H), 4.52-4.54 (m, 4H), 5.2 (d, 1H, J=12 Hz), 5.32 (d, 1H, J=17.25 Hz), 6.0 (m, 1H), 6.77 (s, 2H), 6.85 (s, 1H); 13C NMR (75 MHz, CDCl3) δ 56.3, 65.6, 70.3, 111.2, 113.6, 118.4, 119.7, 133.7, 134.4, 147.8, 149.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258175B2
Source datasetuspto-grants-2012_09
ORD IDord-12c51837408845f39c5ef8eaa7a6e5dc
Source noteuspto-grants-2012_09