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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413656생성일: 2026년 10월 24일

Nitric Acid → 2-Amino-4,6-bis(2-methylbutan-2-yl)phenol

https://huagongshe.com/ko/reaction/413656

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물2,4-Di-tert-pentylphenolHCID 8455—
반응물Potassium FormateHCID 2735122—
촉매Sodium NitriteHCID 23668193—
용매WaterHCID 962—
용매Propyl AcetateHCID 7997—
생성물2-Amino-4,6-bis(2-methylbutan-2-yl)phenolHCID 1491800086.1%

반응 단계

2,4-Di-tert-pentylphenol (93.8 g, 0.4 mol), sodium nitrite (0.6 g, 0.009 mol), 60 mL of water, and 300 mL of propyl acetate were stirred mechanically in a one liter flask at 15-20°. Nitric acid (37.8 g of 70% acid, 0.42 mol) was added slowly via dropping funnel over 30 min keeping the temperature between 25 and 300. The mixture was then stirred vigorously for an additional hour before draining off the lower aqueous phase. The organic layer was washed with a solution of 21 g of sodium bicarbonate in 300 mL of water, passed through 9 g of activated charcoal, and concentrated under reduced pressure to an oil. Palladium catalyst (5 g of 5% Pd/C, 50% wet with water) was added to the oily nitrophenol dissolved in 240 mL of isopropyl alcohol. The mixture was heated with a 55° water bath before slowly adding over 1 h a solution of potassium formate (135 g, 1.6 mol) in 130 mL of water while keeping the temperature under 65°. After stirring an additional hour at 55-60°, the mixture was diluted with 300 mL of propyl acetate and 200 mL of warm water and filtered to remove catalyst. The catalyst was washed with 75 mL of propyl acetate and 75 mL of water. The combined propyl acetate layer was separated, washed with water and then brine, concentrated, and diluted with 200 mL of heptane to crystallize the product. After filtering and drying, 85.9 g (86%) of 2-amino-4,6-di-tert-pentylphenol were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06569612B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-6cf20a4539964ea58c9bc16ab787bc93
출처 메모uspto-grants-2003_05