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HRID 35772作成日:2026年10月24日

4-Chloro-3,5-dimethylphenol → 3-Chloro-6-hydroxy-2,4-dimethylbenzaldehyde

https://huagongshe.com/ja/reaction/35772

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-3,5-dimethylphenolHCID 2723—
反応物Methane, dichloromethoxy-HCID 21004—
触媒Titanium TetrachlorideHCID 24193—
溶媒DichloromethaneHCID 6344—
生成物3-Chloro-6-hydroxy-2,4-dimethylbenzaldehydeHCID 3335082—

反応条件

温度2 °C

反応手順

A solution of 4-chloro-3,5-dimethylphenol (16 g, 0.1 mole) in dichloromethane (100 ml) was stirred and cooled to 2° C. in an ice bath. Titanium tetrachloride (35 g, 0.18 mole) was added dropwise over a period of 10 minutes and dichloromethylmethyl ether (11.5 g, 0.1 mole) was added slowly to the dark red solution, the temperature being kept below 10° C. throughout. After the solution had been stirred at 5° C. for 30 minutes the temperature was allowed to rise and to remian at 20° C. for 30 minutes. Finally the solution was warmed at 35° C. for 15 minutes and then poured into ice water (200 ml). The mixture was shaken vigorously until almost colourless and then the dichloromethane layer was separated and the aqueous phase was extracted with more dichloromethane (2×50 ml). The combined organic layers were washed with water thoroughly (4×200 ml) and then dried over anhydrous magnesium sulphate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure using a rotary evaporator. The product, 3-chloro-6-hydroxy-2,4-dimethylbenzaldehyde was isolated as a white solid (13 g, 70%), mp 89°-90° C. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 2.40 (3H, s); 2.64 (3H, s); 6.71 (1H, s); 10.23 (1H, s); 11.91 (1H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04767879
出典データセットuspto-grants-1988_08
ORD IDord-03a3d8e6f5e2415dab5fceeb87bf006a
出典メモuspto-grants-1988_08