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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1478397생성일: 2026년 10월 25일

Potassium Carbonate → 1-tert-butyl 2-methyl 3-phenyl-1H-pyrrole-1,2-dicarboxylate

https://huagongshe.com/reaction/1478397

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Phenylboronic AcidHCID 66827—
반응물1-tert-butyl 2-methyl 3-bromo-1H-pyrrole-1,2-dicarboxylateHCID 44189803—
촉매Tetrabutylammonium BromideHCID 74236—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물1-tert-butyl 2-methyl 3-phenyl-1H-pyrrole-1,2-dicarboxylateHCID 9038613765.9%

반응 단계

To a solution of 1-tert-butyl 2-methyl 3-bromo-1H-pyrrole-1,2-dicarboxylate (17.6 g, 57.9 mmol) in toluene (200 mL) and water (200 mL) was added potassium carbonate (64.0 g, 463 mmol), followed by phenylboronic acid (10.6 g, 87.0 mmol) and tetrabutylammonium bromide (1.68 g, 5.21 mmol). The reaction mixture degassed for 10 min with nitrogen and then tetrakis(triphenylphosphine)palladium (1.34 g, 1.16 mmol) was added. The resulting slurry was degassed with nitrogen for 30 min and then heated to reflux for 16 h. The reaction mixture was concentrated under reduced pressure to remove water and toluene. Water was then added to the residue and the mixture extracted by ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography using CombiFlash (REDISEP®, silica gel, 80 g, 20% EtOAc/hexanes) to obtain 1-tert-butyl 2-methyl 3-phenyl-1H-pyrrole-1,2-dicarboxylate (11.5 g, 65.9%) as a tan solid. 1H NMR (400 MHz, CD3OD) δ ppm: 1.60 (s, 9H), 3.79 (s, 3H), 6.40 (d, J=3.4 Hz, 1H), 7.37 (m, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09403834B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-d0cc616d177942f88b47f003bb49788b
출처 메모uspto-grants-2016_08