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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878539Generated: October 30, 2026

Benzyl Alcohol → 2-[5-(benzyloxy)-1H-pyrazol-1-yl]pyridine-4-carbonitrile

https://huagongshe.com/reaction/878539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 178510213HCID 178510213—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-[5-(benzyloxy)-1H-pyrazol-1-yl]pyridine-4-carbonitrileHCID 8672551121.7%

Reaction Steps

To a solution of 2-(5-hydroxy-1H-pyrazol-1-yl)pyridine-4-carbonitrile (186 mg, 1 mmol), phenylmethan-1-ol (216 mg, 2 mmol), and PPh3 (523 mg, 2 mmol) in THF (10 mL) was added dropwise DIAD (402 mg, 2 mmoL) at 0° C. under N2. Then the mixture was stirred at rt overnight. Water was added, and the reaction mixture was extracted with EtOAc, then washed with water and brine. The organic phase was dried, concentrated, and purified by prep-HPLC to afford the title compound (60 mg). 1H NMR (400 MHz, CDCl3): δ 5.25 (2H, s), 5.75 (1H, d, J=2.0 Hz), 7.36-7.44 (5H, m), 7.57 (1H, d, J=2.0 Hz), 8.04 (1H, s), 8.71 (1H, d, J=5.2 Hz). [M+H] Calc'd for C16H12N4O, 277; Found, 277.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987461B2
Source datasetuspto-grants-2015_03
ORD IDord-12acf0745fa547779dcbecb611478e55
Source noteuspto-grants-2015_03