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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576414Generated: October 31, 2026

Water → 3-Hydroxy-5-semicarbazono-2-styrylcyclopent-1-eneheptanoic acid

https://huagongshe.com/reaction/1576414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSemicarbazide hydrochlorideHCID 11236—
Reactant3-Hydroxy-5-oxo-2-styrylcyclopent-1-eneheptanoic acidHCID 68135699—
SolventEthanolHCID 702—
SolventPyridineHCID 1049—
Product3-Hydroxy-5-semicarbazono-2-styrylcyclopent-1-eneheptanoic acidHCID 68147716—

Reaction Steps

A solution of 2 parts of semicarbazide hydrochloride in 3 parts of water is combined with a solution of 2 parts of 3-hydroxy-5-oxo-2-styrylcyclopent-1-eneheptanoic acid dissolved in 2.95 parts of pyridine and 15.8 parts of ethanol. The resulting solution is allowed to stand for about 16 hours at room temperature. Then the crystalline precipitate is filtered, washed with an aqueous 80% ethanol solution and then with water. After drying, the material is recrystallized from boiling isopropanol to afford pale yellow crystals of 3-hydroxy-5-semicarbazono-2-styrylcyclopent-1-eneheptanoic acid, melting at about 208°-210°, and displaying, in potassium bromide, an infrared absorption spectrum with maxima at about 3480, 1720, 1693 and 1586 reciprocal centimeters. That compound further displays, in methanol, an absorption band in the ultraviolet spectrum at about 355 millimicrons with a molecular extinction coefficient of about 54,000 and is characterized by the following structural formula ##SPC20##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03980700
Source datasetuspto-grants-1976_09
ORD IDord-15d21edc54b549d89a1b9cbd9f634f8b
Source noteuspto-grants-1976_09