HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → N-({4-[(4-Fluorophenyl)methyl]morpholin-2-yl}methyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(morpholin-2-ylmethyl)acetamide | HCID 10241064 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-({4-[(4-Fluorophenyl)methyl]morpholin-2-yl}methyl)acetamide | HCID 10683176 | 78.9% |
Reaction Steps
A mixture of 2-acetylaminomethylmorpholine (7.0 g), 4-fluorobenzyl chloride (12 g), potassium carbonate (56 g), potassium iodide (1 g), and methyl ethyl ketone (100 ml) is refluxed with stirring for 17 hours. The reaction mixture is filtered and the filtrate is concentrated under reduced pressure. The residue is diluted with water and extracted with chloroform. The organic layer is separated, washed successively with water and saturated aqueous sodium chloride solution, and dried over magnesium sulfate. The solvent is distilled off under reduced pressure, and the residue is recrystallized from toluene to give the title compound (9.3 g), mp 120°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04870074 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-1e6ab4cb163145839771db2808f111a3 |
| Source note | uspto-grants-1989_09 |