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HRID 258210作成日:2026年10月27日

Phenol → 5-t-Amyl-t-butylsalicylaldehyde

https://huagongshe.com/reaction/258210

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物Sulfuric AcidHCID 1118—
反応物ChloroformHCID 6212—
反応物Sodium HydroxideHCID 14798—
反応物2-tert-Butyl-4-(2-methylbutan-2-yl)phenolHCID 14765852—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物5-t-Amyl-t-butylsalicylaldehydeHCID 1973702837%

反応手順

4-t-amyl-2-t-butylphenol (53 g, 0.24 mole) was dissolved in 150 ml absolute ethanol in a 1 L round-bottom flask equipped with a water-cooled condenser. Sodium hydroxide (96 g, 2.4 moles) was dissolved in 100 ml water, and the hot solution was added to the solution of phenol. Chloroform (57 g, 0.48 mole) was added in 1 ml portions over a 45-minute period. The resulting yellow-brown mixture was stirred 1 hour as it cooled to ambient temperature. The mixture was diluted into 500 ml of 1M sulfuric acid and extracted with 200 ml chloroform. The organic layer was isolated in a separatory funnel and dried over anhydrous magnesium sulfate. The mixture was filtered and rotoevaporated to a thick syrup The yield was 37%. The IR spectrum of the crude product showed a characteristic aldehyde carbonyl absorption. The product was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05266283
出典データセットuspto-grants-1993_11
ORD IDord-4bfee79dc30e44a88d9d7ff7271cc9e6
出典メモuspto-grants-1993_11