HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Aminophenyl)(4-fluorophenyl)methanone → 1-(4-Aminophenyl)-1-(4-fluorophenyl)-2-propyn-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Aminophenyl)(4-fluorophenyl)methanone | HCID 577826 | — |
| Reactant | HCID 178420940 | HCID 178420940 | — |
| Reactant | HCID 178463197 | HCID 178463197 | — |
| Solvent | Acetylene | HCID 6326 | — |
| Product | 1-(4-Aminophenyl)-1-(4-fluorophenyl)-2-propyn-1-ol | HCID 87613472 | — |
Reaction Steps
Referring now to FIG. 2, wherein one non-limiting approach to the 1-(4-aminophenyl)-1-(4-fluorophenyl)-2-propyn-1-ol is presented, 4,4′-difluorobenzophenone (7) is reacted with a secondary amine HNR′″R″″ to give the 4-amino-4′-fluorobenzophenone 8, where R′″ and R″″ may be the same as R36 and R37, respectively, as set forth and claimed herein. Acetylide anion, for example, sodium acetylide in acetylene saturated dimethylformamide, is added to the carbonyl of 4-amino-4′-fluorobenzophenone 8 to give, upon aqueous workup, 1-(4-aminophenyl)-1-(4-fluorophenyl)-2-propyn-1-ol 9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07527754B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-1a5dcfb5600647a4b7ac5e22e5269b9e |
| Source note | uspto-grants-2009_05 |