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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350075Generated: October 25, 2026

Sodium Chloride → HCID 23025008, compound

https://huagongshe.com/reaction/350075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium hydrideHCID 24758—
Reactant3-Phenoxybenzyl chlorideHCID 93291—
ReactantHCID 178469912HCID 178469912—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 23025008HCID 2302500877.3%

Reaction Steps

3-Phenoxybenzyl chloride (11.32 g) and ethyl 3-phenyl-1H-pyrazole-4-carboxylate (11.30 g) were dissolved in N,N-dimethylformamide (100 ml). Sodium hydride (60%, oily, 2.49 g) was added to the solution at 0° C., and the solution was stirred at room temperature for 20 hours. The reaction mixture was poured into saturated aqueous sodium chloride solution, which was extracted with ethyl acetate. The ethyl acetate layer was washed with water, then with saturated aqueous sodium chloride solution, dried (MgSO4), then concentrated. The residue was subjected to silica gel column chromatograpy, and an oily substance was obtained from the fraction eluted with ethyl acetate-hexane (1:2, volume ratio). A mixture of the oily substance obtained, potassium hydroxide (8.53 g) and ethanol (150 ml) was refluxed for 5 hours. After the reaction solvent was removed under reduced pressure, water was added to the mixture, then the mixture was acidified using 1N hydrochloric acid. The colorless crystals obtained were collected by filtration to yield 1-(3-phenoxybenzyl)-3-phenyl-1H-pyrazole-4-carboxylic acid (14.83 g, yield: 77%). This was recrystallized from acetone-hexane. Melting point: 148–149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-c83fe56e18464b4baef3edeaba735e7d
Source noteuspto-grants-2007_02