Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667355Generated: October 25, 2026

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

https://huagongshe.com/reaction/1667355

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydrazinobenzenesulfonic acidHCID 66825—
Reactant7-Methyl-8-oxononanoic acidHCID 22266823—
SolventAcetic AcidHCID 176—
SolventMethanol--water (1/1)HCID 22242641—
Product6-(2,3-dimethyl-5-sulfo-3H-indol-3-yl)hexanoic acidHCID 59855422—

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044203B2
Source datasetuspto-grants-2011_10
ORD IDord-f6a651a0128f4f3b8e959c2a44e0274c
Source noteuspto-grants-2011_10