HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842469Generated: October 26, 2026
Triphenylphosphine → 1-Bromo-3,5-di-tert-butylbenzene
https://huagongshe.com/reaction/842469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Bromo-3,5-di-tert-butylbenzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376411B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-d912ae16451644feb51544ea85485f46 |
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| Source note | uspto-grants-2002_04 |
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