HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2,6-dimethyl-N-(2-furoyl)-N-propargyl-aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | 2,6-dimethyl-N-prop-2-ynyl-aniline | HCID 299705 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-dimethyl-N-(2-furoyl)-N-propargyl-aniline | HCID 13150472 | 89% |
Reaction Steps
15.9 g (0.1 mol) of 2,6-dimethyl-N-propargylaniline and 8 g (0.1 mol) of pyridine were heated to the boil in 100 ml of tetrahydrofuran, and 13 g (0.1 mol) of furan-2-carboxylic acid chloride were added carefully. The reaction mixture was stirred under reflux for 15 minutes and then concentrated by distilling off the solvent in vacuo. The residue was taken up in methylene chloride and the methylene chloride mixture was washed with water. The organic phase was separated off, dried over sodium sulphate and concentrated. After triturating with petroleum ether, the residue crystallized. 22.5 g (89% of theory) of 2,6-dimethyl-N-(2-furoyl)-N-propargyl-aniline of melting point 109°-112° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04385069 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-99ec2719e8ce4d6a8e8ef0b654369bc5 |
| Source note | uspto-grants-1983_05 |