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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982016Generated: October 24, 2026

Iodoethane → HCID 20068980, compound

https://huagongshe.com/en/reaction/982016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantCarbon DisulfideHCID 6348—
ReactantChloroacetoneHCID 6571—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant3-OxobutyronitrileHCID 75579—
ReactantSodiumHCID 5360545—
SolventDimethylformamideHCID 6228—
ProductHCID 20068980HCID 20068980—

Reaction Steps

To a suspension of 10.5 g of sodium salt of cyanoacetone in 200 ml of dimethylformamide 9.0 ml of carbon disulphide are gradually added while stirring cooling in ice and keeping under nitrogen, succeeded by 4.5 g of sodium hydride dispersion. After stirring for an hour with cooling, 8.4 ml of chloroacetone are added dropwise under the same reaction conditions. After stirring for another hour, 0.4 g of powdered NaOH are added and finally, after again stirring for another 0.5 hour, 8.0 ml of ethyl iodide under the same conditions. After stirring, the reaction mixture for again another hour and leaving to stand overnight it is poured 1 l of ice water and extracted with diethyl ether. The organic phase is washed with water three times, dried, treated with charcoal, filtered and evaporated. After recrystallisation from isopropanol, the residue yields the desired product in a yield of 9.54 g; melting-point 51°-52° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994485
Source datasetuspto-grants-1991_02
ORD IDord-5ca4d5a75a124d0a8296a3c6089d58fd
Source noteuspto-grants-1991_02