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HRID 649694作成日:2026年10月24日

2,4,6-Trimethylphenol → 3,4,5-Tribromo-2,4,6-trimethyl-2,5-cyclohexadienone

https://huagongshe.com/ja/reaction/649694

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylphenolHCID 10698—
反応物BromineHCID 24408—
反応物3,5-Dibromo-2,4,6-trimethylphenolHCID 13108681—
反応物3,5-Dibromo-4-(bromomethyl)-2,6-dimethylphenolHCID 13954660—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Sodium DiacetateHCID 23662384—
生成物3,4,5-Tribromo-2,4,6-trimethyl-2,5-cyclohexadienoneHCID 20142051—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04740636
出典データセットuspto-grants-1988_04
ORD IDord-8c3c9c6ff7fa470bab4e3dcb32e8886c
出典メモuspto-grants-1988_04