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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918446Generated: October 26, 2026

N-phenyl-3-(phenylthio)acrylamide → HCID 86617324, compound

https://huagongshe.com/reaction/1918446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-phenyl-3-(phenylthio)acrylamideHCID 68865691—
ReactantHCID 86617325HCID 86617325—
SolventChloroformHCID 6212—
ProductHCID 86617324HCID 86617324—

Reaction Conditions

Temperature50 °C

Reaction Steps

N-phenyl-3-(phenylthio)acrylamide (2.0 g) was dissolved to chloroform (10 ml), and 7.8 ml of tetrafluoroboric acid triethyloxonium—dichloromethane 1 mol/L solution was added thereto dropwise under ice-cooling. It was stirred for one hour at room temperature, 50° C. for two hours and for five hours under heat refluxing. After cooling, ice-water was added to the reaction solution, then the chloroform layer was separated. The chloroform layer was washed with water, dried and distilled off the solvent. The residue was subjected to silica gel column chromatography (hexane/ethyl acetate=15/1) to obtain ethyl N-phenyl-3-(phenylthio)acrylimidate (0.15 g) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618329B2
Source datasetuspto-grants-2013_12
ORD IDord-c1deb334433c4a7dbd43c00886223fde
Source noteuspto-grants-2013_12