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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081144Generated: November 1, 2026

Dimethylformamide → HCID 19780828, compound

https://huagongshe.com/reaction/2081144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19780818HCID 19780818—
SolventWaterHCID 962—
ProductHCID 19780828HCID 19780828—

Reaction Steps

0.35 g of sodium hydride (50% dispersion in white oil) is added to 40 ml of dimethylformamide while stirring. 2.9 g of ethyl 2-{2-chloro-5-[3,6-dihydro-2,6-dioxo-4-trifluoromethyl-1(2H)-pyrimidinyl]-benzoyloxy}-2-methyl-propionate [sic] are added portionwise as the solid. After completion of the addition the mixture is stirred at room temperature for a further hour. 1.2 g of allyl bromide are now added in one portion. The reaction mixture is stirred at room temperature for 18 hours and thereafter introduced into 100 ml of water at 0° C. The mixture is extracted twice with 150 ml of ethyl acetate each time. The organic phases are washed once with 100 ml of saturated sodium chloride solution, dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue is purified by chromatography over silica gel with ethyl acetate/n-hexane (1:4). There is obtained ethyl 2-{2-chloro-5-[3,6-dihydro-2,6-dioxo-3-(2-propenyl)-4 -trifluoromethyl-1(2H)-pyrimidinyl]-benzoyloxy}-2-methyl-propionate as an oil;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05183492
Source datasetuspto-grants-1993_02
ORD IDord-8a3af44c642b4a4298e33f71417b24fc
Source noteuspto-grants-1993_02