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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 579260Erstellt: 26. Oktober 2026

Toluene → (p-Tolylsulphonyl)acetone

https://huagongshe.com/reaction/579260

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktChloroacetoneHCID 6571—
EduktSodium p-toluenesulfinateHCID 2723791—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
Produkt(p-Tolylsulphonyl)acetoneHCID 7932788,5%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a 100 ml volume three-necked flask, sodium p-toluenesulfinate (20-a) (9.25 g), tetrabutylammonium bromide (1.65 g), toluene (29 g), and chloroacetone (21-a) (5.0 g) were added, and stirred at 65° C. for 1.25 hours. To the mixture, water (10 g) was added, and stirred for 4 hours. After the mixture was cooled to room temperature, the organic layer was separated, and the aqueous layer was extracted with toluene 2 times. The organic layers were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to column chromatography (chloroform: ethyl acetate=20:1) to give 9.749 g of 1-(4-methylphenylsulfonyl)-2-propanone (7-2-4).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040709B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-5d738568e1d94134bc55bf290598a5a9
Quellennotizuspto-grants-2015_05