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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514382Generated: October 27, 2026

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

https://huagongshe.com/reaction/514382

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 numberUS09107916B2
Source datasetuspto-grants-2015_08
ORD IDord-8112b22090da45c3a7a072575a9c8da0
Source noteuspto-grants-2015_08