تفاعل #58920

ord-02854ddf1583494d8386c11c20c29345

معادلة التفاعل

O=Cc1ccc([N+](=O)[O-])cc1
4-nitrobenzaldehyde
O=C1CSC(=O)N1
1,3-thiazolidine-2,4-dione
C1CCNCC1
piperidine
O=C1NC(=O)C(=Cc2ccc([N+](=O)[O-])cc2)S1
5-(4-nitrobenzylidene)-1,3-thiazolidine-2,4-dione
المردود 59.2%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةunder reflux for 24 hrs
  3. 3
    تركيزThe reaction mixture was concentrated
  4. 4
    غسيلThe obtained residue was washed with ethanol

الإجراء التجريبي

A mixture of 4-nitrobenzaldehyde (15.1 g), 1,3-thiazolidine-2,4-dione (11.70 g), piperidine (1.70 g) and ethanol (300 mL) was heated under reflux for 24 hrs. The reaction mixture was concentrated. The obtained residue was washed with ethanol to give 5-(4-nitrobenzylidene)-1,3-thiazolidine-2,4-dione as yellow crystals (14.8 g, yield 59%). Recrystallization thereof from acetone-hexane gave pale-yellow prism crystals. melting point: 272-273° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07423159B2uspto-grants-2008_09