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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683805Generated: November 1, 2026

Diethyl Ether → HCID 67692481, compound

https://huagongshe.com/reaction/1683805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1-BromopropaneHCID 7840—
ReactantSodium hydrideHCID 24758—
Reactant5-(4-Chloro-phenyl)-2,4-dihydro-pyrazol-3-oneHCID 4778793—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67692481HCID 67692481103.3%

Reaction Steps

To a suspension of 0.22 g (5.5 mmol) of 60% oily sodium hydride in 10 ml of anhydrous dimethylformamide was added dropwise a solution of 1.0 g (4.5 mmol) of 3-(4-chlorophenyl)-4, 5-dihydropyrazol-5-one in dimethylformamide (5 ml) at 0° C. After 30 minutes of stirring at room temperature, 0.83 g (6.7 mmol) of 1-bromopropane 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 resulting 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 1.1 g of the object compound as a colorless oil (yield 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639776
Source datasetuspto-grants-1997_06
ORD IDord-32c937485dbf4b1fa3a8ee6e05edccc2
Source noteuspto-grants-1997_06