HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 23454854, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 5-(1-Chloro-2-methyl-2-nitropropyl)-2H-1,3-benzodioxole | HCID 23454839 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 23454854 | HCID 23454854 | 89% |
Reaction Steps
A mixture of 7.0 g of 1-(3,4-methylenedioxyphenyl)-1-chloro-2-methyl-2-nitropropane, 7.7 g of 70% perchloric acid, 2.8 g of 10% palladium-carbon and 100 ml of ethanol is shaken at room temperature for 3 hours in hydrogen gas atmosphere under 3 atmospheres. After the reaction, insoluble materials are removed by filtration, and the filtrate is condensed. The residue is dissolved in ethyl acetate, and the solution is washed with water, a saturated sodium bicarbonate solution and a saturated sodium chloride solution, successively. The washed solution is dried and then evaporated to remove solvent. 5.4 g of 1-(3,4-methylenedioxyphenyl)-2-methyl-2-nitropropane are thereby obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04276304 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-bfac1b3d2d884b7dbc198abab3a85a5f |
| Source note | uspto-grants-1981_06 |