HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethoxyacetyl chloride → 3-Ethoxymethyl-4-methyl-1,2,4-triazoline-5-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethoxyacetyl chloride | HCID 84189 | — |
| Reactant | N-Methylhydrazinecarbothioamide | HCID 2723853 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-Ethoxymethyl-4-methyl-1,2,4-triazoline-5-thione | HCID 86733223 | 65.8% |
Reaction Steps
Ethoxyacetyl chloride (57 g) was added slowly to a stirred solution of 4-methylthiosemicarbazide (53.5 g) in dry pyridine (500 ml) at 0°-5°. The mixture was allowed to attain room temperature and stirring was continued for 18 hours. Following concentration under reduced pressure the residue was treated with a solution of sodium (21.4 g) in ethanol (500 ml) and the mixture was heated under reflux for 24 hours. Following concentration and acidification with hydrochloric acid a solid was obtained. After partial concentration the solid was collected and recrystallised from ethyl acetate to give 3-ethoxymethyl-4-methyl-1,2,4-triazoline-5-thione (53 g) m.p. 137°-138°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04284640 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-4566ce51ad4a4094918416dd3f5c614a |
| Source note | uspto-grants-1981_08 |