HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 7-Amino-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 7-(Benzhydrylideneamino)-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one | HCID 86625613 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Amino-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one | HCID 11681190 | — |
Reaction Steps
A solution of 7-(benzhydrylideneamino)-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one (5.72 g, 12 mmol) in tetrahydrofuran (150 ml) is treated with 2M HCl solution (150 ml) and allowed to stir at room temperature for 1 hour. The solution is basified with 17% ammonia solution (150 ml), and the mixture is extracted with ethyl acetate (3×200 ml). The organic extracts are combined, dried (MgSO4), filtered and concentrated to afford a yellow suspension. The suspension is triturated with hexanes to afford the title compound as a pale yellow solid, which is isolated by filtration and dried in vacuo overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732435B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-eb3fa833e9984931ac0a2ad081535a12 |
| Source note | uspto-grants-2010_06 |