HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,3-Dimethoxy-benzamidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | 2,3-Dimethoxybenzonitrile | HCID 21862 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,3-Dimethoxy-benzamidine | HCID 3700994 | — |
Reaction Steps
To a solution of 20 g 1,1,1,3,3,3-hexamethyldisilazane in 150 ml dry ether was added 5 mL 2.4M n-butyllithium in hexane. After 10 min at room temperature, 16.3 g 2,3-dimethoxybenzonitrile was added in one portion and the mixture was kept at room temperature for 16 h. The reaction mixture was then poured onto excess 3N HCl. The aqueous layer was separated, basified with 50% NaOH and the product was extracted three times with 10% methanol in methylene chloride. The combined organic extracts were dried over potassium carbonate and the solvents removed in vacuo to afford 2,3-dimethoxybenzamidine as a glassy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646281 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-d77aed33f0414035a9d400eea285924e |
| Source note | uspto-grants-1997_07 |