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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451086Generated: October 30, 2026

Acetic Acid → HCID 10586568, compound

https://huagongshe.com/reaction/1451086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAllyl iodideHCID 11166—
ReactantEthyl-4-acetamidobenzoateHCID 220420—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 10586568HCID 1058656869%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of ethyl-4-acetylaminobenzoate (Coneglio, L. Rend Acad. Sci. Napoli [3] 1931, 36, 56-60) (2.07 g, 0.01 mol) and palladium acetate (1.12 g, 0.005 mol) in dry toluene (17 mL) was heated at reflux for 0.75 h under nitrogen. The solution was cooled to 60° C., the toluene was decanted, and the residue was washed with fresh toluene. The combined filtrates were heated at reflux for 3 h, the precipitate was collected by filtration, and mixed with the previous residue. The combined greenish residues were dried under vacuum for 3 h. To this residue, glacial acetic acid (40 mL) and allyl iodide (8.40 g, 0.05 mol) were added and the mixture was stirred at room temperature for 16 h. The palladium was removed by filtration through Celite and the filtrate was concentrated. The residue was passed through a column of silica gel using 1:1 ethyl acetate:hexane as eluent to give 0.85 g (69%) of ethyl-4-acetylamino-3-allylbenzoate as a white powder, mp 127°-128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602277
Source datasetuspto-grants-1997_02
ORD IDord-19ea8c4b355d4e05851ad93642b79ab2
Source noteuspto-grants-1997_02