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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453315Generated: October 31, 2026

Benzyl Bromide → HCID 14631589, compound

https://huagongshe.com/reaction/1453315

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, 3H), 2.56 (q, J=7.8 Hz, 2H), 5.13 (s, 2H), 6.84 (d, J=8.3 Hz, 1H), 7.04 (dd, J=8.3, 2.3 Hz, 1H), 7.32 (m, 1H), 7.38 (m, 3H), 7.47 (d, J=7.9 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-0cf76d229e6c4dcaa493e14794b5338b
Source noteuspto-grants-2009_01