Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453057Generated: October 31, 2026

2-Propylphenol → 4-Bromo-2-propylphenol

https://huagongshe.com/reaction/1453057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PropylphenolHCID 12570—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventChloroformHCID 6212—
Product4-Bromo-2-propylphenolHCID 22134510—

Reaction Steps

2-propylphenol (3.0 g, 0.022 mol) was dissolved in CHCl3 (100 mL) and magnetically stirred at room temperature. To this solution was added a solution of Tetrabutyl ammonium tribromide (10.68 g, 0.022 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 yellow oil (4.54 g). 1H NMR (CDCl3): δ 1.00 (t, J=8.10 Hz, 3H), 1.52 (m, 2H), 2.50 (t, J=4.56 Hz, 2H), 4.95 (s, 1H), 6.72 (d, J=2.07 Hz 1H)), 6.80 (s, 1H), 6.85 (d, J=2.07 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-bee6b274d0f04c67a11a778ea3fc3a67
Source noteuspto-grants-2009_01