Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960216Generated: November 1, 2026

Thiophenol → HCID 69128191, compound

https://huagongshe.com/reaction/1960216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantSodiumHCID 5360545—
ReactantHCID 69128190HCID 69128190—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 69128191HCID 6912819124.4%

Reaction Steps

N-ethoxycarbonyl-3-(phenylthio)acrylamide (1.20 g) was dissolved to acetonitrile (30 ml), then carbon tetrabromide (2.83 g) and triphenylphosphine (2.23 g) was added thereto and heat refluxing for three hours. The reaction mixture was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (hexane:ethyl acetate20:1) to obtain light yellow oil. It was dissolved to DMF (10 ml), then sodium salt of thiophenol (0.63 g) was added thereto under ice cooling and stirred at room temperature for two hours. t-Butyl methyl ether (100 ml) was added to the reaction mixture, washed successively with 1N aqueous sodium hydroxide solution, water and aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered off inorganic salt and concentrated under reduced pressure. The residue was purified by medium pressure preparative high performance liquid chromatography to obtain phenyl N-ethoxycarbonyl-3-(phenylthio)thioacrylimidate (0.40 g) as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410316B2
Source datasetuspto-grants-2013_04
ORD IDord-94aa161be0ff47e7aaa174041abffd2b
Source noteuspto-grants-2013_04