HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetone → HCID 13670889, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetone | HCID 7678 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 54365084 | HCID 54365084 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13670889 | HCID 13670889 | 4.8% |
Reaction Steps
3 g (10 mmol) of 2-benzyloxybenzylidenenitroacetone in 15 ml of ethanol are heated under reflux with 1.34 g (10 mmol) of phenylacetone and 770 mg (10 mmol) of ammonium acetate for 1.5 hours. The mixture is cooled and concentrated. The residue from evaporation is taken up in ethyl acetate, and the solution is washed with water, dried and concentrated. The resulting residue from evaporation is purified through a column of volume 150 ml, stationary phase silica gel and mobile phase toluene/ethyl acetate 10:1. The pure fractions are combined, concentrated and crystallized using ether. 0.2 g of yellow crystals, of melting point 189° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791122 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-295368fdae204d59b40f418259a4b211 |
| Source note | uspto-grants-1988_12 |