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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44275Erstellt: 27. Oktober 2026

Triethylamine → 3-(Methylsulfanyl)-2-oxo-2,3-dihydro-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/44275

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-AminobenzonitrileHCID 13396—
EduktEthyl (methylthio)acetateHCID 78199—
EduktTert-Butyl hypochloriteHCID 521297—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(Methylsulfanyl)-2-oxo-2,3-dihydro-1H-indole-5-carbonitrileHCID 12351490—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 4-amino-benzonitrile (84.64 mmoles) in DCM (200 ml) under a nitrogen atmosphere, at −78° C., there is added, dropwise, tBuOCl (84.64 mmoles) dissolved in 20 ml of DCM and then, after 10 minutes, ethyl(methylsulphanyl)acetate (84.64 mmoles) dissolved in 20 ml of DCM is added dropwise to the reaction mixture. After stirring for one hour at −78° C., triethylamine (0.152 mol) is added dropwise. The reaction mixture is stirred at ambient temperature for one hour. Water is added and the phases are then separated. The organic phase is washed with water and then with saturated aqueous NaCl solution. The organic phase is dried over sodium sulphate, filtered and evaporated to dryness. The residue is taken up in ethyl ether and aq. 2M HCl solution is added. After stirring overnight, the yellow precipitate is filtered off and dried in vacuo to yield the title product, which is used directly in the next reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541412B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-5927259c609b482ea10f5450258020d5
Quellennotizuspto-grants-2013_09