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HRID 844824作成日:2026年10月27日

6-tert-Butyl-m-cresol → 5-tert-Butyl-4-hydroxy-2-methylbenzaldehyde

https://huagongshe.com/reaction/844824

反応式

関与物質

役割名称HCID仕込み量
反応物6-tert-Butyl-m-cresolHCID 6937—
反応物ChlorobenzeneHCID 7964—
反応物Methane, dichloromethoxy-HCID 21004—
触媒Titanium TetrachlorideHCID 24193—
溶媒WaterHCID 962—
生成物5-tert-Butyl-4-hydroxy-2-methylbenzaldehydeHCID 11286988—

反応条件

温度5 °C

反応手順

Chlorobenzene (100 mL) and 2-tert-butyl-5-methylphenol (20.6 gm, 125 mmol) were combined and the mixture stirred and cooled to 5° C. Titanium tetrachloride (27.5 mL) and dichloromethyl methyl ether (19 mL, 210 mmol) were added separately and simultaneously over 45 minutes while holding the reaction temperature between 4 and 7° C. The resulting mixture was stirred at 0-5° C. for 3 hours. Water (100 mL) was cautiously added over 18 minutes to the reaction mixture while holding the temperature below 14° C. The mixture was extracted with ethyl acetate (200 mL) and the resulting organic layer was extracted with 12% hydrochloric acid (2×75 mL). The combined aqueous acid layers were diluted with water (50 mL) and back extracted with ethyl acetate (100 mL). This extract was combined with the first ethyl acetate extract and the whole extracted with 15% KOH (3×100 mL). The KOH extracts were combined and the pH adjusted to 3 with 37% hydrochloric acid (62.8 gm). The resulting mixture was extracted with 1:1 ethyl acetate/toluene (2×150 mL). These organic extracts were combined and back extracted with water (2×50 mL) and the organic solution concentrated to approximately 75 mL. 5-tert-Butyl-4-hydroxy-2-methylbenzaldehyde seed crystals were added and the mixture stirred and cooled to 25° C. The mixture was filtered and the product washed with toluene (30 mL) and vacuum dried at 40° C. to give 5-tert-butyl-4-hydroxy-2-methylbenzaldehyde (1): 15 g (78 mmol, 62%): mp: 168-170° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06380400B1
出典データセットuspto-grants-2002_04
ORD IDord-dc5ca3b8c1da46b8bbb7066813cf4476
出典メモuspto-grants-2002_04