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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53327Generated: October 29, 2026

Acrylamide → HCID 67635981, compound

https://huagongshe.com/reaction/53327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylamideHCID 6579—
ReactantTriethylamineHCID 8471—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantHCID 54363139HCID 54363139—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 67635981HCID 6763598159.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl 3-[3-bromo-5-[(4-fluorophenyl)hydroxymethyl]phenyl]-2-propenoate (9.50 g), acrylamide (2.67 g), palladium(II) acetate (0.306 g), tri-o-tolylphosphine (0.763 g) and triethylamine (3.80 g) in acetonitrile (10 ml) was heated to 100° C. for 4 hours under an atmosphere of nitrogen and then cooled. Water (150 ml) and dichloromethane (150 ml) was added and the mixture was warmed with stirring to disperse the solid residue. The mixture was cooled and filtered, and the solid was dissolved in hot isopropanol (500 ml). The solution was filtered hot using a filter aid, and the filtrate was concentrated until crystallisation commenced. An equal volume of ether was added and the mixture was allowed to cool. The solid was filtered off and dried to give the title compound (5.50 g), m.p. 197°-199° C. Found: C,68.55; H,5.17; N,4.01. C21H20FNO4 requires C,68.28; H,5.46; N,3.79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618941
Source datasetuspto-grants-1997_04
ORD IDord-bdc0c8ecc8f345fe9cfcea771486fa4d
Source noteuspto-grants-1997_04