HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 21434698, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 3-chloro-3-oxopropionate | HCID 118931 | — |
| Reactant | N-Phenylbenzenecarboximidohydrazide | HCID 18947651 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21434698 | HCID 21434698 | — |
Reaction Steps
A solution of 38 g. (0.227 mole) of the hydrochloride of benzimidic acid phenyl hydrazide, 25 ml. (0.166 mole) of α-chloroformyl acetic acid ethyl ester and 47.5 ml. (0.335 mole) of triethylamine in 420 ml. of methylene chloride is kept at room temperature for about 3 hours, and to it is subsequently added a solution of 38 ml. (0.271 mole) of triethylamine and 25 ml. (0.166 mole) of α-chloroformyl acetic acid ethyl ester in 30 ml. of methylene chloride. The resulting mixture is stirred for about 4 hours and allowed to stand overnight at room temperature. 48 Grams of the crude intermediate compound of formula V, namely 5-carbethoxymethyl-1,3-diphenyl-1,2,4-triazole is so obtained, which is used as such for the subsequent hydrolysis step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024149 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-04f5c52152d248d9894dc2f8ee5a5abf |
| Source note | uspto-grants-1977_05 |