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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351023Erstellt: 25. Oktober 2026

Diphenyl disulfide → 4-[(4-Sulfophenyl)disulfanyl]benzenesulfonic acid

https://huagongshe.com/reaction/351023

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiphenyl disulfideHCID 13436—
EduktChlorosulfonic acidHCID 24638—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[(4-Sulfophenyl)disulfanyl]benzenesulfonic acidHCID 38595479,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of phenyl disulfide (4.36 g, 20 mmol) in dichloromethane (40 mL) at 0° C. is added a solution of chlorosulfonic acid (4.64 g, 2.95 mL, 40 mmol) in dichloromethane (60 mL) dropwise. The mixture is stirred at 0° C. for 1 hour followed by 1.5 hours at room temperature. The reaction mixture is concentrated to dryness in vacuo and the residue is partitioned between diethyl ether and water. The water phase is separated, made basic with 2N aqueous sodium hydroxide and concentrated in vacuo to half the volume. The resulting solution is refrigerated overnight. The precipitate formed overnight is discarded, the filtrate is concentrated further in vacuo until a solid started to appear. The mixture is placed in the refrigerator for 2 hours. The mixture is treated with ethanol, the solid formed is filtered, washed with ethanol twice and dried under high vacuum overnight at room temperature to give 6.0 g of 4,4′-dithiobisbenzenesulfonic acid as a white solid: [M−1]−=398.8.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07183304B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-de02f5b7f4f9441383bb33967f59cfaf
Quellennotizuspto-grants-2007_02