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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360412Generated: October 30, 2026

Ammonium Hydroxide → HCID 66958785, compound

https://huagongshe.com/reaction/1360412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 66958280HCID 66958280—
SolventMethanolHCID 887—
ProductHCID 66958785HCID 66958785—

Reaction Steps

A solution of ethyl 1-benzyl-5-(2-methylpropyl)-1H-pyrazole-3-carboxylate (30 g) in methanol (60 mL) was treated with ammonium hydroxide (60 mL) according to a modification of the method described in Part D of Examples 1-4. The reaction was heated for 14 hours. At the end of the reaction, the methanol was removed under reduced pressure, and the remaining solution was extracted with tert-butyl methyl ether (3×). The combined extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. Toluene was added twice and removed under reduced pressure to remove residual water. Hexane was added to the residue; crystals formed and were isolated by filtration, washed with hexane, and air-dried overnight to provide 6.93 g of 1-benzyl-5-(2-methylpropyl)-1H-pyrazole-3-carboxamide as small, off-white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879849B2
Source datasetuspto-grants-2011_02
ORD IDord-4654c9d4b6204d73af4369e1751eaa9f
Source noteuspto-grants-2011_02