HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649694Generated: October 26, 2026
2,4,6-Trimethylphenol → 3,4,5-Tribromo-2,4,6-trimethyl-2,5-cyclohexadienone
https://huagongshe.com/reaction/649694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trimethylphenol | HCID 10698 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3,5-Dibromo-2,4,6-trimethylphenol | HCID 13108681 | — |
| Reactant | 3,5-Dibromo-4-(bromomethyl)-2,6-dimethylphenol | HCID 13954660 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Diacetate | HCID 23662384 | — |
| Product | 3,4,5-Tribromo-2,4,6-trimethyl-2,5-cyclohexadienone | HCID 20142051 | — |
Reaction Steps
The preparation of a halogenated phenol such as 4-bromomethyl-3,5-dibromo-2,6-dimethylphenol (tribromomesitol) can involve the following sequence: bromination of 2,4,6-trimethylphenol (mesitol) with 2 moles of bromine in acetic acid to prepare 3,5-dibromo-2,4,6-trimethylphenol (dibromometisol) which is isolated by precipitation with water. K. Auwers & F. Rapp, Ann., 302, 153-71 (1898) and O. Jacobsen, Ann., 195, 265-92 (1879); the dibromomesitol is brominated in acetic acid sodium acetate buffer at low temperatures to afford an intermediate, 3,4,5-tribromo-2,4,6-trimethyl-2,5-cyclohexadienone, which is isolated by fast precipitation with water and filtration; this solid slowly rearranges to tribromomesitol at room temperature, more quickly at higher temperatures. K. Fries & E. Brandes, Ann., 542, 48-77 (1939). This procedure to prepare tribromomesitol is complex and not industrially viable.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04740636 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-8c3c9c6ff7fa470bab4e3dcb32e8886c |
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| Source note | uspto-grants-1988_04 |
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