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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097966Generated: November 1, 2026

Acetic Anhydride → 5-[2-(2,4-Dichloro-phenyl)-acryloyl]-1H-pyridin-2-one

https://huagongshe.com/reaction/1097966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant5-[2-(2,4-Dichloro-phenyl)-acetyl]-1H-pyridin-2-oneHCID 57421352—
SolventDichloromethaneHCID 6344—
Product5-[2-(2,4-Dichloro-phenyl)-acryloyl]-1H-pyridin-2-oneHCID 57421353—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-[2-(2,4-dichloro-phenyl)-acetyl]-1H-pyridin-2-one (800 mg) in CH2Cl2 (2.8 ml) was added N,N,N′N′-tetramethyldiaminomethane (896 mg). The mixture was cooled to 0° C. and acetic acid anhydride (0.64 ml) was added. The mixture was stirred at 0° C. for 10 min and at room temperature for 4 h. The solvent was evaporated under reduced pressure. The residue was dissolved in EtOAc and washed with water. The organic phase was concentrated to dryness to give the title compound (857 mg) as a light brown solid that was used for the next step without further purification. MS (m/e, ISP neg. ion)=291.9 [M−H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143280B2
Source datasetuspto-grants-2012_03
ORD IDord-9eb087d8d4904096ad54cd8946564c37
Source noteuspto-grants-2012_03