HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → N-benzyl-4-(p-fluorobenzoylmethyl)-4-piperidinyl hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Cerium(III) chloride | HCID 24636 | — |
| Reactant | 2-Bromo-1-(4-fluorophenyl)ethan-1-one | HCID 96749 | — |
| Reactant | HCID 23002992 | HCID 23002992 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-benzyl-4-(p-fluorobenzoylmethyl)-4-piperidinyl hydrobromide | HCID 89727103 | 34% |
Reaction Steps
Anhydrous cerium chloride (0.99 g, 4.0 mmol) and sodium iodide (1.8 g, 12.0 mmol) are added to 10 ml of anhydrous tetrahydrofuran as a solvent to form a suspension. Dissolving 0.87 g (4.0 mmol) of 2-bromo-1-(4-fluorophenyl)-ethanone and 0.76 g (4.0 mmol) of N-benzyl-4-piperidone in 10 ml of anhydrous tetrahydrofuran, and the solution is added dropwise to the above suspension and reacting at room temperature for 2 hours. Operating according to the post-treatment procedure in General Method three, and a salt is formed by acidifying with hydrobromic acid/ethanol solution, which is recrystallized in ethyl acetate/ethanol to obtain 0.58 g of a white crystal, with yield of 34.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501778B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-8078834df52440d4b7b825ec14080e2f |
| Source note | uspto-grants-2013_08 |