Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27283Generated: October 29, 2026

Water → 1-Ethylenedioxy-2-(6-carboxyhexyl)-3-nitromethyl-cyclopentane

https://huagongshe.com/reaction/27283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-(6-Carboxyhexyl)-3-nitromethyl-cyclopentan-1-oneHCID 23344559—
SolventEthylene GlycolHCID 174—
SolventBenzeneHCID 241—
Product1-Ethylenedioxy-2-(6-carboxyhexyl)-3-nitromethyl-cyclopentaneHCID 70589214—

Reaction Steps

The solution of 2-(6-carboxyhexyl)-3-nitromethyl-cyclopentan-1-one, methyl ester (14 g.) in benzene (200 ml.), ethylene glycol (16.1 ml.), p-toluenesulphonic acid (0.315 g.), is heated to boiling for 16 hours. The reaction water is separated in a Marcusson apparatus. The mixture is washed with an aqueous saturated NaHCO3 -solution (50 ml.), then with water to neutrality, dried over sodium sulphate and the solvent is evaporated in vacuo. From the oily residue, by chromatography on silica (300 g.) and elution with benzene/ethyl acetate (6:1), 13 g. of 1-ethylenedioxy-2-(6-carboxyhexyl)-3-nitromethyl-cyclopentane, methyl ester, are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220798
Source datasetuspto-grants-1980_09
ORD IDord-844ea57a042f4a99b757d9b37d4ac6c2
Source noteuspto-grants-1980_09