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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858638Generated: October 30, 2026

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

https://huagongshe.com/reaction/858638

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, 3 H), 2.65 (q, J=7.6 Hz, 2 H), 5.09 (d, J=4.8 Hz, 1 H), 7.06 (s, 1 H), 7.09 (d, J=11.9 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-a085a84b8088407ab7e6903044f6e125
Source noteuspto-grants-2006_12