Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,2-Dichloro-4-(1-chloroethyl)benzene | HCID 108296 | — |
| Reactant | HCID 54312548 | HCID 54312548 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20361951 | HCID 20361951 | — |
Reaction Steps
25.2 g of 3-methyl-4-ethylpyrazol-5-one were added in portions to a suspension of 10.0 g (0.22 mol) of sodium hydride in 200 ml of absolute dimethylformamide. After the evolution of H2 had ceased, 41.8 g (0.2 mol) of α-methyl-3,4-dichlorobenzyl chloride were added dropwise to the reaction solution. The mixture was then stirred for 2 hours at 60° C, the solvent was distilled off in vacuo and the residue was taken up in water and acidified with dilute acetic acid. The crude product thereby obtained was recrystallized from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04005215 |
|---|
| Source dataset | uspto-grants-1977_01 |
|---|
| ORD ID | ord-f821f5ac53d245bbb8e2fadeb511e98c |
|---|
| Source note | uspto-grants-1977_01 |
|---|
