HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → N-(4-(1-Piperidinyl)phenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Piperidin-1-yl)aniline dihydrochloride | HCID 23366940 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-(1-Piperidinyl)phenyl)acetamide | HCID 732499 | — |
Reaction Steps
A solution of N-(4-aminophenyl)piperidine dihydrochloride (2.49 g) and triethylamine (5.6 g) in dichloroform (30 ml) was ice-cooled and to this was added dropwise acetyl chloride (1.42 ml). After stirred at room temperature for 30 minutes, water (10 ml) was added to the mixture and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off and then the residue was recrystallized from ethyl ether to obtain N(4-acetylaminophenyl)piperidine (2 g) as colorless crystals, m.p. 150°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580883 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-45b0e8bf45724a65aa6aa2fdba130a55 |
| Source note | uspto-grants-1996_12 |