Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457355Generated: October 31, 2026

Sulfuric Acid → 5-Bromo-2-tert-butylphenol

https://huagongshe.com/reaction/1457355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactanttert-ButanolHCID 6386—
Reactant3-BromophenolHCID 11563—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
Product5-Bromo-2-tert-butylphenolHCID 10331382—

Reaction Steps

To a solution of 29.46 g (170.3 mmol) of 3-bromophenol distilled) and 16.41 g (20.9 ml, 221.3 mmol) of t-butanol in 100 ml of carbon tetrachloride was added 20.0 ml of conc. sulfuric acid. The clear, colorless solution turned a dark magenta color and became hot. The solution was cooled in water (ambient temperature) and allowed to stir at room temperature for 84 hours. The reaction mixture was neutralized with sat. aqueous NaHCO3 solution (pH -7.0), partitioned between 300 ml of water and 500 ml of dichloromethane, and the organic and aqueous layers were separated. The aqueous phase was washed with 2×500 ml-portions of dichloromethane. All organic phases were combined, washed with 400 ml of brine solution, dried over MgSO4, filtered and concentrated in vacuo to a purple oil. Purification by flash chromatography (silica, 5% ethyl acetate in hexane) followed by kugelrohr distillation yielded the title compound as a clear, slightly yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05847160
Source datasetuspto-grants-1998_12
ORD IDord-7e033941c6ea45c8ac9cbf8589a26e12
Source noteuspto-grants-1998_12