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HRID 13274생성일: 2026년 10월 24일

Sodium Carbonate → t-Butyl 2-(2-fluoro-5-nitro-phenyl)-pyrrole-1-carboxylate

https://huagongshe.com/ko/reaction/13274

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
반응물Sodium BicarbonateHCID 516892—
반응물1-(tert-Butoxycarbonyl)-2-pyrroleboronic AcidHCID 2734321—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물t-Butyl 2-(2-fluoro-5-nitro-phenyl)-pyrrole-1-carboxylateHCID 23145764—

반응 단계

1.1 g of tetrakis-triphenylphosphine palladium and 4.2 g of sodium carbonate were added to a solution of 4.3 g of 3-bromo-4-fluoro-nitrobenzene and 5.0 g of 1-(t-butoxycarbonyl)pyrrole-2-boronic acid in a mixture of 130 ml of dimethoxyethane and 22 ml of water, and the reaction liquid was heated overnight under reflux. Aqueous saturated sodium bicarbonate was added to the reaction liquid, and this was extracted with ethyl acetate. The organic layer was washed with water and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=20/1) to obtain the entitled compound as a yellow oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5b2c7caafde048c49c5bbc8275c188f1
출처 메모uspto-grants-2010_06