HuagongsheHuagongshe Chemistry Print Report · For research reference only
2'-Hydroxyacetophenone → 2-Methyl-2-(4-nitrophenoxymethyl)-4-oxochroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2'-Hydroxyacetophenone | HCID 8375 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 1-(4-Nitrophenoxy)propan-2-one | HCID 308507 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methyl-2-(4-nitrophenoxymethyl)-4-oxochroman | HCID 15613910 | 54.6% |
Reaction Steps
2 g of o-hydroxyacetophenone, 2.85 g of 4-nitrophenoxyacetone, 2 g of pyrrolidine and 280 mg of p-toluenesufonic acid monohydrate were dissolved in 10 ml of toluene, and the mixture was heated under reflux for 3 hours in apparatus equipped with a water separator. At the end of this time, the reaction mixture was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue was subjected to silica gel column chromatography eluted with a 3:1 by volume mixture of benzene and ethyl acetate, to afford 2.5 g of the title compound as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04873255 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-c398bb4a97a04741b689d7d5447f9001 |
| Source note | uspto-grants-1989_10 |