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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858859Generated: October 31, 2026

Benzyl Bromide → HCID 14631589, compound

https://huagongshe.com/reaction/858859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-ethylphenolHCID 87877—
SolventDimethylformamideHCID 6228—
ProductHCID 14631589HCID 14631589569.5%

Reaction Steps

Potassium carbonate (21.6 g, 0.16 mol) followed by benzyl bromide (6.2 mL, 52 mmol) were added to a solution of 4-bromo-2-ethyl-phenol (1.6 g, 7.9 mmol, from step 1 of Example B(98)) in DMF (75 mL). The mixture was stirred for 20 hours and then partitioned between 1N HCl and EtOAc. The organic layers were washed with brine, dried over Na2SO4 and concentrated. The crude yellow oil was purified by flash column chromatography (hexanes) to give the desired product (13.1 g, 87%). 1H NMR (400 MHz, CDCl3): δ 1.20 (t, J=7.6 Hz, 3 H), 2.56 (q, J=7.8 Hz, 2 H), 5.13 (s, 2 H), 6.84 (d, J=8.3 Hz, 1 H), 7.04 (dd, J=8.3, 2.3 Hz, 1 H), 7.32 (m, 1 H), 7.38 (m, 3 H), 7.47 (d, J=7.9 Hz, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-3b51f4a0e3f54fd9bb3be0813e147a4a
Source noteuspto-grants-2006_12