HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Oxopropyl)amine → N-Acetylmethyl-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Oxopropyl)amine | HCID 215 | — |
| Reactant | Nicotinoyl chloride | HCID 82604 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Acetylmethyl-nicotinamide | HCID 19612493 | — |
Reaction Steps
To a suspension of 40 g (0.370 mol) of aminoacetone in 500 ml of dry dichloromethane, 50 g (0.350 mol) of nicotinoyl chloride was added dropwise at room temperature under a nitrogen atmosphere. The mixture was refluxed 5 h followed by stirring overnight at room temperature. The colorless precipitate was collected by filtration and dissolved in 400 ml of water. After basification with ammonia the aqueous solution was extracted with 3×400 ml of dichloromethane. The combined organic phases were treated with charcoal and dried over magnesium sulphate. Removal of the solvent in vacuo gave a colorless solid, 73. Yield: 30.0 g (0.170 mol, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04866077 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-ddc656a779784665b0312ad81a54134b |
| Source note | uspto-grants-1989_09 |