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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360411Generated: October 31, 2026

Benzylhydrazine dihydrochloride → HCID 66958280, compound

https://huagongshe.com/reaction/1360411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylhydrazine dihydrochlorideHCID 146540—
ReactantPotassium AcetateHCID 517044—
Reactantethyl 6-methyl-2,4-dioxoheptanoateHCID 3006751—
ReactantSodiumHCID 5360545—
SolventAcetic AcidHCID 176—
ProductHCID 66958280HCID 66958280—

Reaction Conditions

Temperature10 °C

Reaction Steps

Potassium acetate (49.1 g, 0.500 mol) was added with stirring to a solution of ethyl 6-methyl-2,4-dioxoheptanoate, sodium salt (44.4 g, 0.200 mol), prepared as described in Part A of Examples 1-4, in acetic acid (280 mL). The solution was cooled to 10° C., and benzylhydrazine dihydrochloride (39.0 g, 0.200 mol) was added in portions over a period of ten minutes while the reaction temperature was maintained between 10° C. and 13.5° C. The reaction was stirred for 90 minutes at between 6° C. and 13.6° C., allowed to warm to ambient temperature, stirred overnight, and concentrated under reduced pressure. The residue was partitioned between 2 M aqueous sodium carbonate (900 mL) and tert-butyl methyl ether (600 mL). The aqueous layer was extracted with tert-butyl methyl ether (2×300 mL), and the combined organic fractions were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 56.6 g of ethyl 1-benzyl-5-(2-methylpropyl)-1H-pyrazole-3-carboxylate as an oil orange. The product contained 10 mol % of ethyl 2-benzyl-5-(2-methylpropyl)-2H-pyrazole-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879849B2
Source datasetuspto-grants-2011_02
ORD IDord-6995126a45344fa8a0efea3a49bd204d
Source noteuspto-grants-2011_02