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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1388931생성일: 2026년 10월 26일

Ethyl 4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetate → [4-Methoxy-1-methyl-5-(2-methylbenzoyl)-1H-pyrrol-2-yl]acetic acid

https://huagongshe.com/reaction/1388931

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetateHCID 20469092—
반응물5-(o-Methylbenzoyl)-4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetateHCID 20469113—
반응물5-(o-Methylbenzoyl)-4-methoxy-3-hydroxycarbonyl-1-methylpyrrole-2-acetic acidHCID 20469154—
용매Trifluoroacetic acidHCID 6422—
생성물[4-Methoxy-1-methyl-5-(2-methylbenzoyl)-1H-pyrrol-2-yl]acetic acidHCID 2046908950%

반응 단계

Following substantially the procedures as described in Example 1, Steps C-E, crude ethyl 4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetate is converted to about 16 mmole of 5-(o-methylbenzoyl)-4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetate followed by hydrolysis to 5-(o-methylbenzoyl)-4-methoxy-3-hydroxycarbonyl-1-methylpyrrole-2-acetic acid which in turn is decarboxylated in neat TFA according to procedure of Example 2 to afford an overall 50% yield of 5-(o-methylbenzoyl)-4-methoxy-1-methylpyrrole-2-acetic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04434175
출처 데이터셋uspto-grants-1984_02
ORD IDord-96574269ed3d4b2091a51409e088389a
출처 메모uspto-grants-1984_02