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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1651507Erstellt: 27. Oktober 2026

Bis(2-aminophenyl) disulfide → Bis(2-oxo-3,3-di-methyl-7-indolinyl)disulfide

https://huagongshe.com/reaction/1651507

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis(2-aminophenyl) disulfideHCID 14358—
Edukt2-Bromo-2-methylpropanoyl chlorideHCID 11106049—
LösungsmittelAcetonitrileHCID 6342—
ProduktBis(2-oxo-3,3-di-methyl-7-indolinyl)disulfideHCID 2304981755,2%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

In a stream of nitrogen, 12.4 g of bis(2-aminophenyl)disulfide was added to 100 ml of acetonitrile, and further added thereto was 18.6 g of α-bromo-α-methylpropionic acid chloride. The resulting mixture was heated under reflux for 3 hours. After removal of acetonitrile, 100 ml of ethylene chloride was added to the reaction product, and gradually added thereto was 28 g of anhydrous aluminium chloride at room temperature. After the conclusion of the additional materials, the mixture was heated for 2 hours at 40° C. with vigorous stirring. The reaction mixture was poured into 200 g of ice-cold water containing concentrated hydrochloric acid in order to decompose the aluminium chloride. After the decomposition, 100 ml of chloroform was added to the reaction mixture, and the organic phase was washed with saturated sodium chloride solution three times. The chloroform-ethylene chloride phase was removed, and concentrated to dryness. The product was purified by column chromatography on silica gel to obtain 10.6 g of bis(2-oxo-3,3-di-methyl-7-indolinyl)disulfide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04929540
Quelldatensatzuspto-grants-1990_05
ORD IDord-fb615c9d032245cc9e2fad740f843619
Quellennotizuspto-grants-1990_05