HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → Ethyl 5-(4-chlorobutyl)-1-methyl-1H-pyrazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 6-Chlorohexan-2-one | HCID 82468 | — |
| Product | Ethyl 5-(4-chlorobutyl)-1-methyl-1H-pyrazole-3-carboxylate | HCID 66959070 | — |
Reaction Steps
Ethyl 5-(4-chlorobutyl)-1-methyl-1H-pyrazole-3-carboxylate was prepared from 6-chloro-2-hexanone (50.0 g, 357 mmol) and diethyl oxalate (48.4 mL, 357 mmol) according to the procedure described in Part A of Example 19 using methyl hydrazine (19.0 mL, 357 mmol) in place of ethylhydrazine oxalate. Ethyl 5-(4-chlorobutyl)-1-methyl-1H-pyrazole-3-carboxylate was isolated as a dark oil that was used without purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879849B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-f5d5f6fd0f25403e80e54e95daccd711 |
| Source note | uspto-grants-2011_02 |