Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418708Generated: October 28, 2026

Sodium hydride → HCID 15390573, compound

https://huagongshe.com/reaction/1418708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(4-Hydroxybenzyl)pyrazoleHCID 133412—
ReactantHCID 14480093HCID 14480093—
SolventDimethylformamideHCID 6228—
ProductHCID 15390573HCID 1539057340.9%

Reaction Steps

To a mixture of 10 ml of anhydrous N,N-dimethylformamide and 72 mg of sodium hydride (60% oil dispersion) was added dropwise an anhydrous N,N-dimethyl-formamide (5 ml) solution of 300 mg of 4-(1-pyrazolyl)methylphenol under stirring over 10 minutes. After stirring at room temperature for 1 hour, the mixture was cooled to 5° to 10° C., to which an anhydrous N,N-dimethylformamide (5 ml) solution of 505 mg of 2-(2-pyridyloxy)ethyl p-toluenesulfonate was added dropwise over 30 minutes. The mixture was stirred at room temperature overnight and then at 60° to 70° C. for further 2 hours. The reaction mixture was poured into 50 ml of ice water, which was extracted twice with 30 ml of ethyl acetate. The organic layers were combined, washed with water, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, which afforded 208 mg of 4-(1-pyrazolyl)methylphenyl 2-(2-pyridyloxy)ethyl ether (compound 1). Yield, 41%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883262
Source datasetuspto-grants-1999_03
ORD IDord-3f8b5d72802b41feb5e8734b44eb6f9c
Source noteuspto-grants-1999_03