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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918440Generated: November 2, 2026

Toluene → HCID 69127214, compound

https://huagongshe.com/reaction/1918440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 86709627HCID 86709627—
CatalystDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 69127214HCID 69127214—

Reaction Conditions

Temperature60 °C

Reaction Steps

N-phenylsulfonyl-3-phenylthioacrylamide (0.50 g) was suspended to toluene (10 ml), then thionyl chloride (0.20 ml), triethylamine (0.40 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 (8 ml). DMF (2 ml) solution of sodium salt of thiophenol (0.30 g) was added thereto under ice-cooling, and it was stirred at room temperature for 1.5 hours. Ethyl acetate (80 ml) was added to the reaction mixture, and 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=10:1) to obtain phenyl N-phenylsulfonyl-3-(phenylthio)thioacrylimidate (0.14 g) as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618329B2
Source datasetuspto-grants-2013_12
ORD IDord-25356aa2550143cb959b4e35524590b7
Source noteuspto-grants-2013_12