HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178512120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2,6-Dichlorobenzaldehyde | HCID 6737 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178506607 | HCID 178506607 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178512120 | HCID 178512120 | — |
Reaction Steps
A solution of 2.83 g. of 2,6-dichlorobenzaldehyde and 1-amino-3-(pyrazinylmethyl)guanidine hydriodide from Example 10 in 50 ml. of absolute ethanol and 5.0 ml. of glacial acetic acid is heated at reflux for 4 hours. The cooled solution is made basic by addition of 10N sodium hydroxide and extracted with ether. The ether extract is evaporated to give a residual orange gum which is crystallized from absolute ethanol to give the desired product as colorless crystals, m.p. 168°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04154947 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-22022493b50f42a592f5330ad9a475eb |
| Source note | uspto-grants-1979_05 |