تفاعل #2467993

ord-e303b211dd224814817efa9246fc399b

معادلة التفاعل

C[O-].[Na+]
sodium methoxide
[Na+].[Na+].[S-2]
sodium sulfide
N#CC=C(Cl)c1ccccc1
3-chloro-3-phenylprop-2-enenitrile
N#CCCl
chloroacetonitrile
N#Cc1sc(-c2ccccc2)cc1N
solid
المردود 8.0%
N#Cc1sc(-c2ccccc2)cc1N
3-Amino-5-phenylthiophene-2-carbonitrile
المردود 8.0%

المذيبات

ظروف التفاعل

درجة الحرارة
65°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGagain stirred at 60-70° C. for 2 h
  2. 2
    workup.STIRRINGstirring
  3. 3
    workup.WAITwas continued for 1 h at the same temperature
  4. 4
    أخرىwas allowed to rt
  5. 5
    workup.STIRRINGstirred for 15 min
  6. 6
    أخرىThe solid separated
  7. 7
    ترشيحwas filtered
  8. 8
    غسيلwashed with water
  9. 9
    أخرىdried
  10. 10
    أخرىThe solid was recrystallized from hexane-chloroform

الإجراء التجريبي

To a suspension of sodium sulfide (0.95 g, 12.23 mmol) in DMF (12.5 mL) was added a solution of 3-chloro-3-phenylprop-2-enenitrile (2 g, 12.23 mmol) in DMF (5 mL) at rt for 5 min and stirred the mixture at 60-70° C. for 2 h. Then chloroacetonitrile (0.77 mL, 12.23 mmol) was added dropwise to the reaction mixture and again stirred at 60-70° C. for 2 h. Then, a solution of sodium methoxide (0.66 g, 12.23 mmol) in methanol (5 mL) was added dropwise and stirring was continued for 1 h at the same temperature. The mixture was allowed to rt and poured into cold water and stirred for 15 min. The solid separated was filtered, washed with water and dried. The solid was recrystallized from hexane-chloroform to give the product as a pale brown color solid (150 mg, 8%), nip 158-160° C. 1H NMR (400 MHz, CDCl3): δ 7.52-7.54 (2H, m), 7.37-7.41 (3H, m), 6.75 (1H, s), 4.48 (2H, s); LC-MS (negative ion mode): m/z 199 (M−H)−.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08258119B2uspto-grants-2012_09