HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581460Generated: October 26, 2026
Sulfuric Acid → 5-Bromo-2-tert-butylphenol
https://huagongshe.com/reaction/581460
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 3-Bromophenol | HCID 11563 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-Bromo-2-tert-butylphenol | HCID 10331382 | — |
Reaction Steps
To a solution of 29.5 g (170.3 mmol) of 3-bromophenol in 100 mL of carbon tetrachloride (under a blanket of argon) was added 16.4 g (221.3 mmol) of 2-methyl-2-propanol followed by 20 mL of conc. sulfuric acid. The reaction mixture was allowed to stir at ambient temperature for 3.5 days. The clear, colorless solution turned pink and eventually turned purple in color. The reaction mixture was neutralized with sat. NaHCO3 (aq.) solution and then extracted between water and dichloromethane. The layers were separated and the aqueous phase was washed with dichloromethane. The organic phases were combined and washed with brine, 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 (85-95° C., 2 mm Hg) gave the title compound as a clear, slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05919970 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-1f8784d9fcb24aab97657fcfdfe3091a |
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| Source note | uspto-grants-1999_07 |
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