HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Amino-4'-n-octyl-2',3',5',6'-tetrafluorobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2',3',4',5',6'-Pentafluoro[1,1'-biphenyl]-4-ylamine | HCID 15938617 | — |
| Reactant | HCID 178506867 | HCID 178506867 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Amino-4'-n-octyl-2',3',5',6'-tetrafluorobiphenyl | HCID 15938622 | — |
Reaction Steps
n-Octyllithium in dry ether (9.5 mL) was added slowly to a solution of 4-amino-2′,3′,4′,5′,6′-pentafluorobiphenyl (1.5 g, 5.79 mmol, Example 9) in dry ether (100 mL) at −78° C. The solution was stirred at this temperature for 2 hours and then allowed to warm to room temperature over a period of 5 hours. Hydrochloric acid (3M, 100 mL) was added and a white solid was precipitated from the solution. The solid was filtered and dried. After sublimation, 4-amino-4′-n-octyl-2′,3′,5′,6′-tetrafluorobiphenyl was obtained as a white solid (1.2 g, 63% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902363B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-a3851edf7f04442f9808ef4b8d7676e7 |
| Source note | uspto-grants-2011_03 |