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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51221Erstellt: 24. Oktober 2026

Dichloromethane → 2-(4-Chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one

https://huagongshe.com/de/reaction/51221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt4-ChloroanilineHCID 7812—
EduktTriethyloxonium tetrafluoroborateHCID 2723982—
Edukt5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-oneHCID 12056392—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
Produkt2-(4-Chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-oneHCID 1205639957,8%

Reaktionsschritte

5-Methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-one (0.28 g) was mixed with a 1M methylene chloride solution of triethyloxonium tetrafluoroborate (1 ml) at room temperature. The reaction mixture was stirred for 24 hrs at room temperature then p-chloroaniline (0.25 g) in chloroform (10 ml) was added to the mixture at 0° C. The mixture was stirred at room temperature for 1 hr and then water was added. The separated oil was extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (chloroform-n-hexane, 1/1) to yield 2-(4-chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one (0.21 g) having a melting point of 53-54° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713629B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-cd27c9acc26c47ba8554b42114b3e20a
Quellennotizuspto-grants-2004_03