Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414710Generated: October 31, 2026

Acetic Acid → HCID 22642381, compound

https://huagongshe.com/reaction/2414710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant2-Methyl-N-(4-nitrophenyl)prop-2-enamideHCID 13396419—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
ProductHCID 22642381HCID 2264238172.7%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 114 g of 2-methyl-N-(4-nitro phenyl) acrylamide (0.55 mol) and 92.6 g of Fe powder (1.65 mol=3 mol equiv.) was refluxed in 420 ml of ethanol. While refluxing, 400 ml of acetic acid (6.6 mol=12 mol equiv.) was added. A proper cooling and a safe gas separation were ensured. During the first reaction step a very strong exothermic gas release occurred. After completing of the addition of acetic acid, stirring while refluxing was continued for 60 min. After TLC inspection, 300 ml of ethyl acetate was added and the Fe salts were suction-filtered. The salts were then washed with 1.9 liter of ethyl acetate. While stirring, 138 ml of concentrated HCl (1.65 mol=3 equiv.) was added to the filtrate. The mixture was cooled to 5° C. while stirring. The precipitate was suction-filtered and washed with ethyl acetate. After drying at 40° C., 85 g of N-(4-amino phenyl)-2-methyl acrylamide hydrochloride was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815139B2
Source datasetuspto-grants-2004_11
ORD IDord-34a49608631d46cdb6fed43d99ceb652
Source noteuspto-grants-2004_11