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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478124Generated: October 30, 2026

Acetic Acid → HCID 22642381, compound

https://huagongshe.com/reaction/478124

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.) in 420 ml of ethanol was refluxed. Upon 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 L of ethyl acetate. While stirring, 138 ml of HCl conc. (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 (i.e. 72% versus 117 g theor.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06641970B2
Source datasetuspto-grants-2003_11
ORD IDord-612bc45ba1084c6ab30aad71309f48ff
Source noteuspto-grants-2003_11