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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376739생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 2-(1-pentyl-1H-pyrrol-2-yl)-[1,4]-naphthoquinone

https://huagongshe.com/ko/reaction/376739

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물1,4-NaphthoquinoneHCID 8530—
반응물n-PentylpyrroleHCID 557117—
용매ChloroformHCID 6212—
생성물2-(1-pentyl-1H-pyrrol-2-yl)-[1,4]-naphthoquinoneHCID 1066140126%

반응 단계

6.32 millimol of 1,4-naphthoquinone and 3.16 millimol of N-pentylpyrrole were stirred in 50 ml of chloroform in a round-bottomed flask for 5 hours at room temperature, the reaction being catalysed by addition of a few milligrams of para-toluenesulphonic acid. The reaction medium was diluted with 50 ml of chloroform and then washed four times with 50 ml of water and finally with saturated aqueous NaCl solution. The resulting organic phase was dried over Na2SO4 and then concentrated under vacuum. The product 2-(1-pentyl-1H-pyrrol-2-yl)-[1,4]-naphthoquinone was thus isolated, in the form of an oil, in a yield of 26% after purification by chromatography on a column of silica.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06022379
출처 데이터셋uspto-grants-2000_02
ORD IDord-4cdfb3ea6fd1417dbb2b0b49ac16fede
출처 메모uspto-grants-2000_02