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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683811Generated: November 4, 2026

Diethyl Ether → HCID 67712048, compound

https://huagongshe.com/reaction/1683811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant5-(4-Chloro-phenyl)-2,4-dihydro-pyrazol-3-oneHCID 4778793—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67712048HCID 6771204895%

Reaction Steps

To a suspension of 0.44 g (11 mmol) of 60% oily sodium hydride in 10 ml of anhydrous dimethylformamide was added dropwise a solution of 2.2 g (10 mmol) of 3-(4-chlorophenyl)-4, 5-dihydropyrazol-5-one in dimethyl-formamide (5 ml) at 0° C. After 30 minutes of stirring at room temperature, 2.1 g (11 mmol) of t-butyl bromoacetate was added dropwise, and stirring was continued for another 2 hours. To the reaction solution was added 50 ml of diethyl ether and 50 ml of water, and vigorously agitated. The resultant solution was separated, and the aqueous layer was extracted twice with 50 ml of diethyl ether. The organic layer was combined and washed successively with water and saturated brine solution, and dried over anhydrous sodium sulfate. Then the solvent was evaporated under reduced pressure. The obtained crude product was purified by silica gel column chromatography (n-hexane/ethyl acetate=4/1 (v/v)) to give 3.2 g of the object compound as a colorless oil (yield 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639776
Source datasetuspto-grants-1997_06
ORD IDord-3b4706b467654a4496534eccc689fb6f
Source noteuspto-grants-1997_06