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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360407Generated: October 25, 2026

Ammonium Hydroxide → 1-butyl-5-methyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/1360407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactantethyl 1-butyl-5-methyl-1H-pyrazole-3-carboxylateHCID 66958271—
SolventMethanolHCID 887—
Product1-butyl-5-methyl-1H-pyrazole-3-carboxamideHCID 66958958—

Reaction Steps

A solution of ethyl 1-butyl-5-methyl-1H-pyrazole-3-carboxylate (18.1 g, 86.1 mmol) in methanol (25 mL) was treated with ammonium hydroxide (25 mL) according to a modification of the method described in Part D of Examples 1-4. At the end of the reaction, the methanol was removed under reduced pressure, and the remaining solution was cooled in a refrigerator. A precipitate formed, was isolated by filtration, and was washed with water. The solid (9 g) was recrystallized from hexane (300 mL) and ethyl acetate (30 mL), isolated by filtration, washed with hexane, and air-dried to provide 6.95 g of 1-butyl-5-methyl-1H-pyrazole-3-carboxamide as colorless plates, mp 113.5-114.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879849B2
Source datasetuspto-grants-2011_02
ORD IDord-5065ce42aaab450d84aa5c6470bb1b81
Source noteuspto-grants-2011_02