HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 20335430, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,3-Diethyl 2-acetylpropanedioate | HCID 136365 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (3,4-Dichlorophenyl)hydrazine monohydrochloride | HCID 3084323 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20335430 | HCID 20335430 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 1.3 g of diethyl α-acetyl-malonate, 1.3 g of 3,4-dichlorophenylhydrazine hydrochloride, 0.5 g of sodium acetate, 30 ml of ethanol and 10 ml of water is warmed on the steam cone for 10 minutes. It is diluted with water, extracted with diethyl ether, the extract washed with water, dried and evaporated. The residue is taken up in 50 ml of xylene, the solution distilled for 10 minutes and refluxed for 85 minutes. It is evaporated and the residue triturated with diethyl ether to yield the 1-(3,4-dichlorophenyl)-3-methyl-4-carbethoxy-2-pyrazolin-5-one, melting at 147°-148°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04207317 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-83908b5d650d4c279af527ee4de30ac9 |
| Source note | uspto-grants-1980_06 |