HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-(2,6-Dichlorobenzylideneamino)-3-(2-thenyl)guanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (2-Thienylmethyl)amine | HCID 34005 | — |
| Reactant | Methyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydroiodide | HCID 178504060 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(2,6-Dichlorobenzylideneamino)-3-(2-thenyl)guanidine | HCID 178512116 | — |
Reaction Steps
A solution of 5.85 g. of methyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydriodide and 3.39 g. of 2-(aminomethyl)thiophene in 25 ml. of absolute ethanol is heated under reflux for 16 hours, diluted with water and excess 10N sodium hydroxide is added. After standing, crystallization occurs, and filtration gives 3.50 g. of nearly colorless crystals. Recrystallization from aqueous ethanol gives the desired product as colorless crystals, m.p. 135°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04154947 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-99cc69d1626a41b6ac9ae6c77d9a89d0 |
| Source note | uspto-grants-1979_05 |