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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414229Generated: October 30, 2026

Phenylacetone → HCID 13670889, compound

https://huagongshe.com/reaction/414229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetoneHCID 7678—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 54365084HCID 54365084—
SolventEthanolHCID 702—
ProductHCID 13670889HCID 136708894.8%

Reaction Steps

3 g (10 mmol) of 2-benzyloxybenzylidenenitroacetone in 15 ml of ethanol are heated under reflux with 1.34 g (10 mmol) of phenylacetone and 770 mg (10 mmol) of ammonium acetate for 1.5 hours. The mixture is cooled and concentrated. The residue from evaporation is taken up in ethyl acetate, and the solution is washed with water, dried and concentrated. The resulting residue from evaporation is purified through a column of volume 150 ml, stationary phase silica gel and mobile phase toluene/ethyl acetate 10:1. The pure fractions are combined, concentrated and crystallized using ether. 0.2 g of yellow crystals, of melting point 189° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04791122
Source datasetuspto-grants-1988_12
ORD IDord-295368fdae204d59b40f418259a4b211
Source noteuspto-grants-1988_12