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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506626Generated: October 25, 2026

(+-)-2-Butanol → 2-phenyl-1-(1-phenyl-1H-1,2,3-triazol-5-yl)ethanamine

https://huagongshe.com/reaction/1506626

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-2-ButanolHCID 6568—
ReactantSodium borohydrideHCID 4311764—
Reactant1-phenyl-1H-1,2,3-triazole-5-carbonitrileHCID 84653709—
ReactantHCID 178418336HCID 178418336—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-phenyl-1-(1-phenyl-1H-1,2,3-triazol-5-yl)ethanamineHCID 90281247—

Reaction Steps

To a solution of 9C (280 mg, 1.63 mmol) in tetrahydrofuran (5 mL), benzylmagnesium chloride (2M in THF) (1.23 mL, 2.46 mmol) was added dropwise. After 3 hours, 3 mL of 2-butanol was added to the reaction and sodium borohydride (0.5 g) was added to the mixture by portion. The reaction was monitored by LC/Mass until it was done. Methanol (5 mL) was added to the mixture. The organic layer was washed with brine and extracted with ethyl acetate (50 mL twice). The organic layer was dried with Na2SO4, filtered and concentrated. The crude product was purified by flash column (Rf: 0.3, 3% MeOH/DCM) to provide the desired product. MS (m/z) 265 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09220710B2
Source datasetuspto-grants-2015_12
ORD IDord-55b96b07b7ae4eed898402a7696ec0dc
Source noteuspto-grants-2015_12