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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547512Generated: October 31, 2026

Sodium borohydride → HCID 67198422, compound

https://huagongshe.com/reaction/547512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67196717HCID 67196717—
SolventMethanolHCID 887—
ProductHCID 67198422HCID 6719842269.7%

Reaction Steps

495 mg (1.8 mM) of 4-nitro-1-phenethyl-1H-pyrazole-3-carboxylic acid ethyl ester was dissolved in 5 ml of methyl alcohol, to which 680 mg (18 mM, 13 eq) of sodium borohydride was added dropwise at 0° C., and the resulting mixture was stirred under a nitrogen atmosphere for 1 hour. The solvent was distilled off under reduced pressure, and the resultant was extracted with ethyl acetate and brine. The organic solvent layer was dried over anhydrous sodium sulfate, filtered, and then distilled under reduced pressure. The resulting impure compound was purified by column chromatography (hexane:ethyl acetate=2:1), to obtain 295 mg (66.4%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939550B2
Source datasetuspto-grants-2011_05
ORD IDord-953ef879feef4eeb988aa0ed02b7530b
Source noteuspto-grants-2011_05