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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59732생성일: 2026년 10월 25일

Nitric Acid → 1-Methyl-4-nitropyrrole-2-carboxylic acid

https://huagongshe.com/reaction/59732

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Acetic AnhydrideHCID 7918—
반응물1-Methyl-2-pyrrolecarboxylic acidHCID 81453—
생성물1-Methyl-4-nitropyrrole-2-carboxylic acidHCID 273691519.8%

반응 단계

Acetic anhydride (8 ml, 85 mmol) was treated with nitric acid (1.020 ml, 15.98 mmol) (heating occurred upon addition); the mixture was cooled to RT and slowly added to a suspension of 1-methyl-1H-pyrrole-2-carboxylic acid (2 g, 15.98 mmol) in acetic anhydride (12 ml, 127 mmol) cooled to −30° C. The reaction was stirred at −30° C. for 0.5 hours, then at RT for 20 minutes. The mixture was cooled again to −30° C. to precipitate the desired product. The solid was quickly filtered in a frit funnel cooled in dry ice; after a few minutes at room temperature, the solid became deliquescent and resulted in a thick slurry/solution that was collected in a separate flask. The slurry was cooled at −30° C. and washed twice with a mixture of hexane (5 ml) and (iPr)2O (1 ml). The obtained solid was dried under vacuum, then treated with 2N NaOH till complete dissolution (10 ml) and precipitated again by addition of 37% HCl (20 ml). The solid was filtered, washed with water (10 ml) and finally dried under vacuum for 3 days to yield 1-methyl-4-nitro-1H-pyrrole-2-carboxylic acid (Int. 15) (540 mg, 3.17 mmol, MS/ESI+ 170.9 [MH]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440954B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-fcff824f67a04906980905fecd10c881
출처 메모uspto-grants-2016_09