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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090829Generated: November 1, 2026

Ammonium Chloride → HCID 66778670, compound

https://huagongshe.com/reaction/2090829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 43324083HCID 43324083—
ReactantHCID 178420632HCID 178420632—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66778670HCID 6677867036%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-carbaldehyde (2.6 g) synthesized above in tetrahydrofuran (40 mL) was added dropwise 1M cyclohexylmagnesium bromide tetrahydrofuran solution (15 mL) at 0° C. After stirring at 0° C. for 1 hr, aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate. The extract was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4, volume ratio) to give the title object compound (2.0 g, 36%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-415b24c6aa4c45f4acf492ebfb58b0e9
Source noteuspto-grants-2013_05