HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2,3,4-Trimethoxy-6-methylbenzoyl cyanide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,3,4-Trimethoxy-6-methylbenzoic acid | HCID 13531415 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,3,4-Trimethoxy-6-methylbenzoyl cyanide | HCID 23133651 | 45% |
Reaction Steps
10 ml of thionyl chloride was added to 6.0 g (26.6 mmol) of 2,3,4-trimethoxy-6-methylbenzoic acid, followed by stirring under reflux with heating for 4 hours, and the surplus thionyl chloride was distilled off under reduced pressure. 20 ml of toluene, 8 ml of acetonitrile and 3.1 g (34.5 mmol) of copper(I) cyanide were added, followed by stirring under reflux with heating for 16 hours. After cooling to room temperature, the reaction solution was subjected to filtration on the pad of celite, and the solvent was distilled off under reduced pressure. The crude product was purified by silica gel column chromatography to obtain 2.8 g (yield: 45%) of 2,3,4-trimethoxy-6-methylbenzoyl cyanide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653113B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-be0e7a8b61094bc5bf7903e96a87b913 |
| Source note | uspto-grants-2014_02 |