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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918442Generated: November 1, 2026

Acetanilide → HCID 86617323, compound

https://huagongshe.com/reaction/1918442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetanilideHCID 904—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86617322HCID 86617322—
SolventEthyl AcetateHCID 8857—
ProductHCID 86617323HCID 8661732317%

Reaction Steps

To DMF (3 ml) solution of acetanilide (0.14 g) was added sodium hydride (60% in oil: 0.043 g) under ice-cooling, and DMF (2 ml) solution of phenyl N-phenyl-3-(phenylsulfonyl)acrylimidate (0.30 g) was added dropwise. It was stirred for two hours under ice-cooling and for one hour at room temperature. Ethyl acetate (100 ml) was added to the reaction mixture and was successively washed with water and aqueous saturated sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate, concentrated under reduced pressure. The residue was isolated and purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain phenyl N-phenyl-3-(N′-acetyl-N′-phenylamino)acrylimidate (0.050 g) as yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618329B2
Source datasetuspto-grants-2013_12
ORD IDord-87b00dfab46248f1b0a3b39de71394b4
Source noteuspto-grants-2013_12