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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453089Generated: October 30, 2026

Tetra-n-butylammonium tribromide → 4-Bromo-2-ethyl-6-fluorophenol

https://huagongshe.com/reaction/1453089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetra-n-butylammonium tribromideHCID 23500184—
Reactant2-Ethyl-6-fluorophenolHCID 58762693—
SolventChloroformHCID 6212—
Product4-Bromo-2-ethyl-6-fluorophenolHCID 4509535360%

Reaction Steps

A solution of tetrabutyl ammonium tribromide (4.2 g, 8.6 mmol) in CHCl3 (25 mL) was added to a stirred solution of 2-ethyl-6-fluoro-phenol (1.1 g, 7.9 mmol) dissolved in CHCl3 (25 mL). The reaction mixture was stirred for 24 hrs and then quenched with 5% solution of sodium thiosulfate (30 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 (1 g, 60%). 1H NMR (400 MHz, CDCl3): δ 1.21 (t, J=7.6 Hz, 3H), 2.65 (q, J=7.6 Hz, 2H), 5.09 (d, J=4.8 Hz, 1H), 7.06 (s, 1H), 7.09 (d, J=11.9 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-956768fc54f94e0a9fd3afd8a2786925
Source noteuspto-grants-2009_01