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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842479Generated: October 25, 2026

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

https://huagongshe.com/reaction/842479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant3,5-Di-tert-butylphenolHCID 70825—
SolventAcetonitrileHCID 6342—
Product1-Bromo-3,5-di-tert-butylbenzeneHCID 620136—

Reaction Steps

A 1000 mL three-neck, round-bottom flask was equipped with a mechanical stirrer, a pressure-compensating dropping funnel, and a reflux condenser. A nitrogen gas flow adapter with overpressure valve was attached on top of the reflux condenser. A slight nitrogen flow guaranteed an inert gas atmosphere in the apparatus. The flask was charged with 181 g triphenylphosphine (690 mmol) and 160 mL acetonitrile (HPLC grade). The white suspension was cooled in an ice bath for 15 minutes. While stirring, dropwise addition of 101.5 g bromine (635 mmol) took place within 40 minutes. After bromine addition, the ice bath was removed. 124 g of 3,5-di-tertbutylphenol (601 mmol) and 140 mL acetonitrile were added in one portion. The orange/white suspension converted into an orange solution upon heating. The mechanical stirrer was replaced by an egg-shape stir bar. The solution was stirred at gentle reflux temperature for three hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376412B1
Source datasetuspto-grants-2002_04
ORD IDord-8a4721adaa65478f8561016645ae4af0
Source noteuspto-grants-2002_04