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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333946Generated: October 26, 2026

Sodium Hydroxide → HCID 66835573, compound

https://huagongshe.com/reaction/333946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-2,2-difluoroacetaldehydeHCID 93560—
Reactant2-Diethoxyphosphoryl-1-[4-(4-quinolyl)piperazin-1-yl]ethanoneHCID 86691595—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66835573HCID 6683557310%
Product(E)-4-chloro-4,4-difluoro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-oneHCID 668358527%

Reaction Steps

2-Diethoxyphosphoryl-1-[4-(4-quinolyl)piperazin-1-yl]ethanone (78.3 mg, 0.2 mmol) was dissolved in anhydrous THF (1 ml), NaH was added (12 mg of a 60% dispersion in mineral oil, 0.3 mmol) and the mixture was stirred for 30 minutes at room temperature. 2-Chloro-2,2-difluoro-acetaldehyde (0.3 mmol, the solution of step D) was added, the temperature was raised to 45° C. and stirring was continued for 3 hours. The mixture was diluted with water, basified with 0.1 NaOH and extracted with diethylether (2×). The combined organic phases were washed with 5% sodium bicarbonate solution, water, dried over magnesium sulfate and the solvent was removed under reduced pressure. The raw product was purified by preparative HPLC (gradient of water containing 0.1% ammonia and acetonitrile) to yield (E)-4-chloro-4,4-difluoro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one (5 mg, 0.014 mmol, 7%) and (Z)-4-chloro-4,4-difluoro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one (7 mg, 0.02 mmol, 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-4c1d92d7f5d24620a11bc1003c227871
Source noteuspto-grants-2014_11