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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059384Generated: October 31, 2026

Sodium Chloride → HCID 18670226, compound

https://huagongshe.com/reaction/1059384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-5-nitropyridineHCID 78308—
ReactantEthyl 5-bromo-2,2-dimethylpentanoateHCID 10681333—
SolventDimethylformamideHCID 6228—
ProductHCID 18670226HCID 1867022674.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

5 g of diethyl malonate was dissolved in 30 ml of N,N-dimethylformamide and 1.550 g of sodium hydride (60% oily) was added thereto under ice-cooling. Next, 7.04 g of ethyl 2,2-dimethyl-5-bromopentanoate was added to the reaction mixture and the resulting mixture was stirred at 80° C. for 2 hours. After ice-cooling the reaction mixture again, 1.550 g of sodium hydride (60% oily) was added thereto. After stirring for 25 minutes, 7.4 g of 2-chloro-5-nitropyridine was added and the resulting mixture was stirred at 80° C. for 1.5 hours. After the completion of the reaction, the reaction mixture was poured into a saturated aqueous solution of sodium chloride and repeatedly extracted with ethyl acetate. The extracts were dried over anhydrous sodium sulfate and filtered. The filtrate was distilled under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluted with ethyl acetate/n-hexane) to thereby give 9.71 g of the title compound as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-7afd9708711048aeb3202253eeb146d8
Source noteuspto-grants-2003_02