HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 86745168, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 10944045 | HCID 10944045 | — |
| Reactant | Bis(4-fluorophenyl)(piperidin-4-yl)methanol | HCID 11208889 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86745168 | HCID 86745168 | 141% |
Reaction Steps
A mixture of 4.0 g (0.013 mole) of α,α-bis(4-fluorophenyl)-4-piperidinemethanol, 3.5 g (0.016 mole) of 6-bromo-N,N-dimethylhexanamide, 5.5 g (0.052 mole) of anhydrous sodium carbonate and 0.3 g (0.002 mole) of potassium iodide in 50 mL of N,N-dimethylformamide was stirred at ambient temperature for 16 h. The mixture was poured into 1 L of water and extracted twice with 250 mL of ethyl acetate. The combined ethyl acetate fractions were washed with water and brine, dried (MgSO4) and concentrated under reduced pressure. The residue was converted to the oxalic acid salt, and recrystallized from 2-propanol to yield 4.9 g (71%) of the title compound as a white solid, mp 157°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05057524 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-facb76b8e7424314a65cf62233a9762c |
| Source note | uspto-grants-1991_10 |