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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1667355생성일: 2026년 10월 25일

4-Hydrazinobenzenesulfonic acid → 6-(2,3-dimethyl-5-sulfo-3H-indol-3-yl)hexanoic acid

https://huagongshe.com/reaction/1667355

반응식

참여 물질

역할이름HCID투입량
반응물4-Hydrazinobenzenesulfonic acidHCID 66825—
반응물7-Methyl-8-oxononanoic acidHCID 22266823—
용매Acetic AcidHCID 176—
용매Methanol--water (1/1)HCID 22242641—
생성물6-(2,3-dimethyl-5-sulfo-3H-indol-3-yl)hexanoic acidHCID 59855422—

반응 단계

To a stirred solution of 4-hydrazinobenzenesulfonic acid (Aldrich, 11.25 g, 0.06 mol) in acetic acid (50 ml) was added 7-acetyloctanoic acid (16.7 g, 0.09 mol). The reaction mixture was heated under reflux for 12 hrs. Acetic acid was removed under reduced pressure. The resulting solid was dissolved in methanol and reprecipitated with a saturated solution of potassium hydroxide in isopropanol. The solid was filtered, washed with isopropanol and dried, (8 g, 40%). The analytical sample was obtained by C18 reversed phase column chromatography using water/methanol mixture as solvent, m.p. 250° C. dec; IR ν cm−1=2930, 2597, and 1719. 1H NMR, D2O, δ, 7.8-7.9 (m, 2H, 4-H and 6-H of aromatic protons); 7.6 (d, J=7 Hz, 1H, 7-H of aromatic); 2.2 (t, J=7 Hz, 2H, —CH2—COOH); 1.9-2.1 (m, 2H, alkyl); 1.2-1.6 (a singlet merged in a multiplet, 7H, —CH3, (—CH2)2); 0.6-0.9 (m, 2H, alkyl.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044203B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-f6a651a0128f4f3b8e959c2a44e0274c
출처 메모uspto-grants-2011_10