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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258208생성일: 2026년 10월 25일

Phenol → 3,5-Di-tert-butylsalicylaldehyde

https://huagongshe.com/reaction/258208

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물ChloroformHCID 6212—
반응물2,4-Di-tert-butylphenolHCID 7311—
반응물Sodium HydroxideHCID 14798—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Sulfuric AcidHCID 1118—
생성물3,5-Di-tert-butylsalicylaldehydeHCID 68802333%

반응 단계

2,4-di-t-butylphenol (75 g, 0.36 mole) was dissolved in 200 ml absolute ethanol in a 1 L round bottom flask equipped with a water-cooled condenser. Sodium hydroxide (82 g, 2.0 moles) was dissolved in 80 ml water and added while still hot to the solution of phenol. Chloroform (156 g, 1.31 mole) was added in 2 ml portions over a 45-minute period. The resulting yellow-brown mixture was stirred 1 hour while cooling to ambient temperature. The mixture was diluted with 500 ml of 1M sulfuric acid and extracted with 200 ml of dichloromethane. 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 33%. The IR spectrum of the crude product showed the characteristic aldehyde carbonyl (C=O) stretching frequency at 1648 cm-1. 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-c0a82c355bd7434d9d23b0a5c3d5b7db
출처 메모uspto-grants-1993_11