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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47098생성일: 2026년 10월 24일

2,5-Hexanedione → 3-Sulphamoyl-4-phenoxy-5-(2,5-dimethyl-1-pyrrolyl)-benzoic acid

https://huagongshe.com/ko/reaction/47098

반응식

참여 물질

역할이름HCID투입량
반응물2,5-HexanedioneHCID 8035—
반응물3-Amino-4-phenoxy-5-sulfamoylbenzoic acidHCID 119927—
용매Acetic AcidHCID 176—
생성물3-Sulphamoyl-4-phenoxy-5-(2,5-dimethyl-1-pyrrolyl)-benzoic acidHCID 12883729—

반응 단계

A mixture of 3-sulphamoyl-4-phenoxy-5-aminobenzoic acid (1.54 g=5 mmols; P. W. Feit, J. Med. Chem. 14, 432 (1971)), acetonylacetone (0.57 g=5 mmols) and 10 ml of glacial acetic acid is refluxed under N2 for 30 minutes, the red reaction solution is evaporated in vacuo and freed from residues of glacial acetic acid and water by adding benzene and evaporating azeotropically, the residue is dissolved in acetone, the solution is boiled with silica gel and filtered through a fine filter and the solution is concentrated to 50 ml and, after adding 50 ml of ethyl acetate, freed from acetone residues in vacuo, whereupon crystallisation takes place. After the purification procedure has been repeated, beige-coloured crystals with a melting point of 283°-286° (decomposition) result.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04176190
출처 데이터셋uspto-grants-1979_11
ORD IDord-b4dd32f738804d1ab26ad29360b531ae
출처 메모uspto-grants-1979_11