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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690515Generated: November 2, 2026

Sodium borohydride → Benzyl-(2-phenyl-2H-indazol-3-yl)-amine

https://huagongshe.com/reaction/1690515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66905500HCID 66905500—
SolventEthanolHCID 702—
ProductBenzyl-(2-phenyl-2H-indazol-3-yl)-amineHCID 4511061865.2%

Reaction Steps

Sodium borohydride (245 mg, 6.46 mmol) was added to a suspension of (2-phenyl-2H-indazol-3-yl)-[1-phenyl-methylidene]-amine (480 mg, 1.61 mmol) in ethanol (13 ml) at ambient temperature under an argon atmosphere. The reaction mixture was stirred at ambient temperature for 12 h, poured onto ice water/aqueous NaHCO3 solution 1/1 and extracted two times with iPrOAc. The combined extracts were washed with ice water/brine 1/1 and dried over Na2SO4. After filtration the solvent was removed under reduced pressure, the resulting yellow oil was purified by column chromatography (silica gel, iPrOAc/heptane) to give the title compound (314 mg, 1.05 mmol; 65%) as yellow oil. MS: m/e=300.4 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153663B2
Source datasetuspto-grants-2012_04
ORD IDord-d7550530fd714917983e55437bd6b25c
Source noteuspto-grants-2012_04