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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452999Generated: October 30, 2026

2-Tert-Butylphenol → 4-Bromo-2-tert-butylphenol

https://huagongshe.com/reaction/1452999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-ButylphenolHCID 6923—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventChloroformHCID 6212—
Product4-Bromo-2-tert-butylphenolHCID 97068—

Reaction Steps

2-tert-Butyl-phenol (5 g, 0.033 mol) was dissolved in CHCl3 (100 mL) and magnetically stirred at room temperature. To this solution was added a solution of Tetrabutyl ammonium tribromide (16.05 g, 0.033 mol) in CHCl3 (100 mL). The resulting yellow solution was allowed to stir at room temperature for 1 hour. The reaction was quenched with a 5% solution of sodium thiosulfate (200 mL). The biphasic mixture was stirred for 15 min. The organics were separated and concentrated. The residue was dissolved in EtOAc (100 mL) and washed with water (2×100 mL) and brine (1×100 mL). The organics were dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (silica gel) eluting with 3% EtOAc in Hexanes. The result was a clear oil (6.8 g, 89%) 1H NMR (CDCl3): δ 1.39 (s, 9H), 4.95 (s, 1H), 6.59 (d, J=8.5 Hz 1H), 7.19 (d, J=8.5 Hz, 1H), 7.24 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-5d5159cf39b847878f8120b2ee408d64
Source noteuspto-grants-2009_01