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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360504Generated: October 25, 2026

Methylhydrazine → Ethyl 5-(4-chlorobutyl)-1-methyl-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/1360504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantDiethyl OxalateHCID 7268—
Reactant6-Chlorohexan-2-oneHCID 82468—
ProductEthyl 5-(4-chlorobutyl)-1-methyl-1H-pyrazole-3-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879849B2
Source datasetuspto-grants-2011_02
ORD IDord-f5d5f6fd0f25403e80e54e95daccd711
Source noteuspto-grants-2011_02