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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20200생성일: 2026년 10월 24일

5-((1H-Pyrrol-2-YL)methyl)-1H-pyrrole-2-carbaldehyde → Dipyrromethane

https://huagongshe.com/ko/reaction/20200

반응식

참여 물질

역할이름HCID투입량
반응물5-((1H-Pyrrol-2-YL)methyl)-1H-pyrrole-2-carbaldehydeHCID 16732691—
반응물21H,22H-PorphineHCID 137705241—
생성물DipyrromethaneHCID 14081446%

반응 단계

1-Formyldipyrromethane 2 is the key precursor for the porphine synthesis described herein. Formylation of dipyrromethane via Vilsmeier or Grignard reagent mediated syntheses21 results in multiple byproducts, requiring tedious chromatographic separation for the purification of 1-formyldipyrromethane (2). The TLC and 1H NMR analyses of the crude reaction mixture obtained from Vilsmeier formylation of dipyrromethane showed the presence of three components: starting dipyrromethane (3), 1-formyldipyrromethane (2), 1,9-diformyldipyrromethane (4), and an unknown byproduct (tentatively assigned as a 2-formyldipyrromethane) in a ratio of 7:20:4:1. We were able to separate the desired 2 in 46% yield (without using a tin complexation strategy); however, the purification required lengthy column chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745618B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1ae614c9e1c44c79a850d45cef6482db
출처 메모uspto-grants-2010_06