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HRID 13446생성일: 2026년 10월 23일

Potassium Carbonate → Tert-butyl 4-(4-amino-3-nitrophenoxy)picolinate

https://huagongshe.com/ko/reaction/13446

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물4-Amino-3-NitrophenolHCID 3758882—
반응물tert-Butyl 4-chloropicolinateHCID 11806045—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 4-(4-amino-3-nitrophenoxy)picolinateHCID 22041090—

반응 조건

온도80 °C

반응 단계

Solid anhydrous white powdered KHMDS (2 eq) was suspended in a solution of dimethylformamide. Red crystalline 4-amino-3-nitrophenol (1 eq) was charged to the rapidly stirring solution under an inert atmosphere and the heterogeneous solution was allowed to stir for 2 hours. Then a dimethylformamide solution of tert-butyl 4-chloropyridine-2-carboxylate (1 eq) was added dropwise. Anhydrous powdered potassium carbonate (1.2 eq) was charged to the reaction as an acid scavenger. The purple colored viscous mixture was heated to 80° C. for 12-15 hours until when it was determined to be complete by HPLC. The reaction was evaporated under reduced pressure and diluted with excess ethyl acetate and water. An extraction of the aqueous layer was made with ethyl acetate. The organic layers were combined and washed 4 times with water followed by brine. The organic layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude material was purified by flash silica gel chromatography using an eluent of 1:1 mixture of hexanes to ethyl acetate to give the desired product. MS: MH+=332.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728010B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-00d13c5c1a234708ab4cef80b7b55f27
출처 메모uspto-grants-2010_06