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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858776Generated: October 30, 2026

2-Ethylphenol → 4-Bromo-2-ethylphenol

https://huagongshe.com/reaction/858776

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-EthylphenolHCID 6997—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventChloroformHCID 6212—
Product4-Bromo-2-ethylphenolHCID 8787798.3%

Reaction Steps

A solution of tetrabutyl ammonium tribromide (19.7 g, 41 mmol) in CHCl3 (100 mL) was added to a stirred solution of 2-ethylphenol (5 g, 41 mmol) dissolved in CHCl3 (150 mL). The reaction mixture was stirred for 2 hrs and then quenched with 5% solution of sodium thiosulfate (150 mL). The biphasic mixture was stirred for 30 mins and then the layers were separated. The organic layer was washed with 1N HCl, saturated NaHCO3, brine, dried over Na2SO4 and concentrated. The crude residue was purified by flash column chromatography (0–10% EtOAc in hexanes) to give the desired product (8.1 g, 98%). 1H NMR (400 MHz, CDCl3): δ 1.22 (t, J=7.5 Hz, 3H), 2.60 (q, J=7.5 Hz, 2 H), 6.64 (d, J=8.5 Hz, 1 H), 7.17 (dd, J=8.5, 2.5 Hz, 1 H), 7.24 (d, J=2.5 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-3800e135d698426da5e8beab025e76ff
Source noteuspto-grants-2006_12