HuagongsheHuagongshe Chemistry Print Report · For research reference only
10-phenyl-1H-indeno[1,2-b]quinolin-11-one → 10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 10-phenyl-1H-indeno[1,2-b]quinolin-11-one | HCID 131734054 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-ol | HCID 117606248 | 90% |
Reaction Steps
After dripping 1M phenylmagnesium bromide (20 ml, 20.0 mmol) into the starting material 10-phenyl-1H-indeno[1,2-b]quinolin-11-one (3.07 g, 10.0 mmol) which is dissolved in pure tetrahydrofuran, the mixed solution undergoes reaction for 24 hours at room temperature. Then, the reaction is terminated by adding ammonium chloride solution therein. Finally, 3.47 g of 10,11-diphenyl-11H-indeno[1,2-b]quinolin-11-ol is obtained by filtering the mixed solution to remove precipitates. The percentage yield is 90.0%. 10-diphenyl-11H-indeno[1,2-b]quinolin-11-ol obtained here can be also used as starting materials to produce other 6H-indeno[2,1-b]quinoline derivatives.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09184396B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-594abf8213c144a6941230de9c1dd7e9 |
| Source note | uspto-grants-2015_11 |