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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918439Generated: October 30, 2026

Toluene → HCID 69128554, compound

https://huagongshe.com/reaction/1918439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 69128553HCID 69128553—
CatalystDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 69128554HCID 6912855432.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

Phenyl N-phenyl-3-(phenoxy)thioacrylimidate N-phenyl-3-phenoxyacrylamide (1.5 g) was suspended to toluene (80 ml), then thionyl chloride (0.82 ml), triethylamine (1.8 ml) and one drop of DMF were added thereto at room temperature. The mixture was stirred on the 60° C. oil bath for three hours. Then it was cooled and filtered off the insoluble matter. The filtrate was concentrated under reduced pressure. The residue was dissolved to DMF (80 ml). Sodium salt of thiophenol (0.82 g) was added to it under ice-cooling, and stirred for 2 hours. t-Butyl methyl ether (250 ml) was added to the reaction mixture. It was successively washed with 1N aqueous sodium hydroxide solution, water and aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered off an inorganic salt, concentrated under reduced pressure. The residue was isolated and purified by silica gel column chromatography (hexane:ethyl acetate=20:1) to obtain phenyl N-phenyl-3-(phenoxy)thioacrylimidate (0.28 g) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618329B2
Source datasetuspto-grants-2013_12
ORD IDord-e6690db47f5846b0b53b3af06ba5d725
Source noteuspto-grants-2013_12