HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,6-Trimethoxybenzonitrile → N-HYDROXY-2,4,6-TRIMETHOXY-BENZAMIDINE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,6-Trimethoxybenzonitrile | HCID 75731 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-HYDROXY-2,4,6-TRIMETHOXY-BENZAMIDINE | HCID 5191888 | — |
Reaction Steps
To a suspension of 13.8 g of hydroxylamine hydrochloride in 100 ml of ethanol is added, at a temperature in the region of 15° C., a solution of NaOC2H5 prepared by dissolving 4.3 g of sodium in 100 ml of ethanol. 12 g of 2,4,6-trimethoxybenzonitrile are introduced into the medium, followed by heating at reflux for 41 h before evaporating to dryness. The crystals are washed with water and with dichloromethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534530 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-6d38f2833779447cbd4d3dbb4de43b23 |
| Source note | uspto-grants-1996_07 |