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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420809Generated: November 1, 2026

Water → 1-Allyloxy-2-bromo-4-trifluoromethoxy-benzene

https://huagongshe.com/reaction/1420809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-(trifluoromethoxy)phenolHCID 21584090—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-Allyloxy-2-bromo-4-trifluoromethoxy-benzeneHCID 18782491—

Reaction Steps

To a solution of 2-bromo-4-trifluoromethoxyphenol (Description 11; 8 g, 0.03 mol) and K2CO3 (8.6 g, 0.06 mol) in dimethylformamide (100 ml) was added allyl bromide (4 ml, 0.045 mol). The solution was stirred for 4 h. at room temperature undre nitrogen whereupon water (400 ml) and ethyl acetate (3×100 ml) were added and the combined organic phase was washed with water (200 ml), saturated brine (200 ml), dried (MgSO4) and the solvent removed in vacuo. The residue was purified by chromatography on silica gel (eluting with 5% ethyl acetate in hexane) to give the title compound as a yellow oil 1H NMR (250 MHz, CDCl3) δ4.60 (2H, dt, J 5, 1.6 Hz), 5.33 (1H, dq, J 10.5, 1.4 Hz), 5.48 (1H, dq, J 17.3, 1.6 Hz), 6.04 (1H, m), 6.86 (1H, d, J 9 Hz, 7.13 (1H, dd, J 8.4, 2.7 Hz), and 7.45 (1H, d, J 2.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071927
Source datasetuspto-grants-2000_06
ORD IDord-c0dc39a43ba6403a852b6cebe9d918ef
Source noteuspto-grants-2000_06