HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Ethylenedioxy-2-(6-carboxyhexyl)-3-nitromethyl-cyclopentane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-(6-Carboxyhexyl)-3-nitromethyl-cyclopentan-1-one | HCID 23344559 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-Ethylenedioxy-2-(6-carboxyhexyl)-3-nitromethyl-cyclopentane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04220798 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-844ea57a042f4a99b757d9b37d4ac6c2 |
| Source note | uspto-grants-1980_09 |