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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960199Generated: October 30, 2026

Toluene → HCID 69128554, compound

https://huagongshe.com/reaction/1960199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 69127057HCID 69127057—
CatalystDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 69128554HCID 69128554—

Reaction Conditions

Temperature60 °C

Reaction Steps

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 numberUS08410316B2
Source datasetuspto-grants-2013_04
ORD IDord-353f14f544e142f1aca9fe6ac011ef2a
Source noteuspto-grants-2013_04