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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1075497Erstellt: 26. Oktober 2026

Pyridine → Phenyl vinyl sulfone

https://huagongshe.com/reaction/1075497

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktThionyl ChlorideHCID 24386—
Edukt2-(Phenylsulfonyl)ethanolHCID 30202—
EduktSodium BicarbonateHCID 516892—
LösungsmittelTolueneHCID 1140—
ProduktPhenyl vinyl sulfoneHCID 7966498%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

2-(phenylsulfonyl)ethanol (143.8 g, purity 96.2%, 743 mmol) was added to 71.9 g of toluene, and 30.0 g (38 mmol) of pyridine was added to the mixture. The resulting solution was heated to 60° C., then 110.5 g (929 mmol) of thionyl chloride added over 5 hours at 60 to 70° C., and the mixture was stirred for 2 hours at 70° C. Then, the mixture was diluted with 143.9 g of toluene and cooled to 45° C. Then 303.2 g of 7% sodium bicarbonate solution and 193.4 g of toluene were added, washed separated. Obtained organic layer was mixed with 303.2 g of 7% sodium bicarbonate solution and stirred and separated. 5 g of the organic layer was sampled and subjected to HPLC analysis, which revealed that (β-chloroethylsulfonyl)benzene was obtained in a yield of 98% and phenylvinylsulfone in a yield of 0.7%. (Internal Standard: methyl benzoate).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05902905
Quelldatensatzuspto-grants-1999_05
ORD IDord-9456b4a8742c442b87542d0c5aa9de23
Quellennotizuspto-grants-1999_05