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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylphenolHCID 10698—
ReactantBromineHCID 24408—
Reactant3,5-Dibromo-2,4,6-trimethylphenolHCID 13108681—
Reactant3,5-Dibromo-4-(bromomethyl)-2,6-dimethylphenolHCID 13954660—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSodium DiacetateHCID 23662384—
Product3,4,5-Tribromo-2,4,6-trimethyl-2,5-cyclohexadienoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04740636
Source datasetuspto-grants-1988_04
ORD IDord-8c3c9c6ff7fa470bab4e3dcb32e8886c
Source noteuspto-grants-1988_04