تفاعل #1435701

ord-dd590dc6069b484bbd50972ff09490a8

معادلة التفاعل

C1CCNCC1
piperidine
CC1=CC(=C(C#N)C#N)C=C(C(C)(C)C)O1
2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile
O=Cc1ccc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)s1
5-(4-diphenylamino-phenyl)-thiophene-2-carbaldehyde
CC(C)(C)C1=CC(=C(C#N)C#N)C=C(C=Cc2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)O1
target compound
المردود 50.0%
CC(C)(C)C1=CC(=C(C#N)C#N)C=C(C=Cc2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)O1
2-(2-tert-butyl-6-{2-[5-(4-diphenylamino-phenyl)-thiophene-2-yl]-vinyl}-pyran-4-ylidene)-malononitrile
المردود 50.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    درجة الحرارةThe reaction solution was heated for 24 hours
  3. 3
    درجة الحرارةwhile refluxing
  4. 4
    درجة الحرارةAfter cooling the reaction solution
  5. 5
    ترشيحthe precipitated red solid was filtered
  6. 6
    أخرىrecrystallized with ethanol

الإجراء التجريبي

As shown in the following reaction 3, 0.72 g (3.37 mmol) of (2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile and 1 g (2.81 mmol) of 5-(4-diphenylamino-phenyl)-thiophene-2-carbaldehyde were added into 50 ml of ethanol, and 0.28 g (3.37 mmol) of piperidine was added thereto. The reaction solution was heated for 24 hours while refluxing. After cooling the reaction solution, the precipitated red solid was filtered, and recrystallized with ethanol to obtain 0.79 g of the target compound (Yield 50%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07211335B2uspto-grants-2007_05