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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258211생성일: 2026년 10월 26일

Phenol → 2-Hydroxy-3,5-bis(2-methylbutan-2-yl)benzaldehyde

https://huagongshe.com/reaction/258211

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물ChloroformHCID 6212—
반응물2,4-Di-tert-pentylphenolHCID 8455—
반응물Sodium HydroxideHCID 14798—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물2-Hydroxy-3,5-bis(2-methylbutan-2-yl)benzaldehydeHCID 11065254—

반응 단계

2,4-di-t-amylphenol (70 g, 0.30 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 (149 g, 1.25 mole) was added in 2 ml portions over a 45-minute period. The resulting yellow-brown mixture was stirred 2 hours while cooling to ambient temperature. The mixture was extracted into 400 ml of hexanes and the organic layer rinsed with 400 ml of 1M HCl. 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, and the IR spectrum of the crude product showed the characteristic aldehyde carbonyl stretching frequency. 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-14441e01a68a4210854564d5bc41de9e
출처 메모uspto-grants-1993_11