HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-Cyanomethyl-5-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(Cyanomethyl)-5-methylbenzoic acid | HCID 23084810 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyanomethyl-5-methylbenzamide | HCID 23084702 | — |
Reaction Steps
2-Cyanomethyl-5-methylbenzoic acid (16.3 g) and dimethylformamide (0.1 mL) were suspended in tetrahydrofuran (160 mL), and oxalyl dichloride (12.2 mL) was added dropwise under ice-cooling. After cease of foaming, the solvent was evaporated. The obtained residue was dissolved in tetrahydrofuran, and the solution was added dropwise to 28% aqueous ammonia solution under ice-cooling. After the completion of the reaction, the solvent was evaporated, and the precipitated crystals were collected by filtration to give 2-cyanomethyl-5-methylbenzamide (10.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501412B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-5302a0223cf146c2a418b84a39eda23c |
| Source note | uspto-grants-2009_03 |