Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984331Generated: October 25, 2026

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

https://huagongshe.com/reaction/1984331

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 numberUS07544697B2
Source datasetuspto-grants-2009_06
ORD IDord-e4596f72e52b497ba1a6166ea3572a9c
Source noteuspto-grants-2009_06