Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414357Generated: November 3, 2026

Acetone → HCID 70621761, compound

https://huagongshe.com/reaction/1414357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantIodoethaneHCID 6340—
ReactantHCID 20352737HCID 20352737—
SolventWaterHCID 962—
ProductHCID 70621761HCID 70621761—

Reaction Steps

To 2.89 gms. (0.01 mole) of 1-(p-trifluoroacetamidophenyl)-3-methyl-3-(4-pyridylmethyl)urea [prepared by reacting 1-(p-aminophenyl)-3-methyl-3- (4-pyridylmethyl)urea (Example 6., supra.) with trifluoroacetic anhydride (method of Hickenbottom, Reactions of Organic Compounds, Longmans, London, 1963)] there is added 6.24 gms. (0.04 mole) of ethyl iodide in 50 ml. of dry acetone. The acetone is then stripped and the residue added to 50 ml. of water. The aqueous mixture is warmed to reflux for about 30 minutes and then allowed to stand overnight. The mixture is then stripped of water to give 1-(p-ethylaminophenyl)-4-methyl-3-(4-pyridylmethyl)urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001256
Source datasetuspto-grants-1977_01
ORD IDord-acbe8c4c78e44e0593d70fb8d35bca69
Source noteuspto-grants-1977_01