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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258210생성일: 2026년 10월 26일

Phenol → 5-t-Amyl-t-butylsalicylaldehyde

https://huagongshe.com/reaction/258210

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Sulfuric AcidHCID 1118—
반응물ChloroformHCID 6212—
반응물Sodium HydroxideHCID 14798—
반응물2-tert-Butyl-4-(2-methylbutan-2-yl)phenolHCID 14765852—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물5-t-Amyl-t-butylsalicylaldehydeHCID 1973702837%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05266283
출처 데이터셋uspto-grants-1993_11
ORD IDord-4bfee79dc30e44a88d9d7ff7271cc9e6
출처 메모uspto-grants-1993_11