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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017141Generated: October 26, 2026

1,3,5-Tri-tert-butylbenzene → 1-Bromo-3,5-di-tert-butylbenzene

https://huagongshe.com/reaction/1017141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-Tri-tert-butylbenzeneHCID 15089—
ReactantBromineHCID 24408—
CatalystIronHCID 23925—
Catalysttert-ButylcatecholHCID 77643—
SolventCarbon TetrachlorideHCID 5943—
Product1-Bromo-3,5-di-tert-butylbenzeneHCID 62013646.4%

Reaction Conditions

Temperature5 °C

Reaction Steps

1,3,5-Tri-t-butylbenzene (150 g, 0.6 mol) was dissolved in carbon tetrachloride (300 mL) in a three-necked flask which had been painted black to avoid light and equipped with an overhead stirrer, thermometer and addition funnel under argon. Iron pellets (36 g. 0.64 mol) were added and the slurry was cooled to 5° C. t-Butylcatechol (1.0 g) was added and a solution of bromine (201.6 g, 1.26 mol) in carbon tetrachloride (75 mL) was added over a one hour period. The slurry was stirred for an additional 4 hours at 5° C. and quenched by pouring into ice water. The layers were separated and the organics washed with 10% sodium hydroxide solution. The solution then was washed with salt brine and dried over magnesium sulfate. The solvent was evaporated and the product was distilled under vacuum twice to give 75 g of product which was then recrystallized from heptane to give 47 g of pure product (29% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479424B1
Source datasetuspto-grants-2002_11
ORD IDord-220913932a814915b0fc33d433d1ec05
Source noteuspto-grants-2002_11