تفاعل #2467971

ord-9b488cadbbca4e889ff9f28a4ab35be6

معادلة التفاعل

C[O-].[Na+]
sodium methoxide
COC(=O)CS
methyl thioglycolate
C[O-].[Na+]
sodium methoxide
N#CC=C(Cl)c1ccccc1
3-chloro-3-phenylprop-2-enenitrile
O
water
COC(=O)c1sc(-c2ccccc2)cc1N
solid
المردود 62.9%
COC(=O)c1sc(-c2ccccc2)cc1N
Methyl 3-amino-5-phenylthiophene-2-carboxylate
المردود 62.9%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred the mixture at 60° C. for 2 h
  2. 2
    workup.STIRRINGstirring
  3. 3
    workup.WAITwas continued for 2 h at 60° C
  4. 4
    أخرىwas allowed to rt
  5. 5
    workup.STIRRINGstirred for 15 min
  6. 6
    استخلاصThe solution was extracted with chloroform (3×100 mL)
  7. 7
    غسيلthe combined chloroform layer was washed with water, brine
  8. 8
    تجفيفdried over sodium sulfate
  9. 9
    ترشيحThe solution was filtered
  10. 10
    أخرىevaporated the solvent
  11. 11
    أخرىThe residue was chromatographed over silica gel

الإجراء التجريبي

To a solution of methyl thioglycolate (1 g, 9.43 mmol) in methanol (5 mL) was added a solution of sodium methoxide (0.5 g, 9.43 mmol) in methanol (5 mL) and stirred for 0.5 h. To the above mixture, a solution of 3-chloro-3-phenylprop-2-enenitrile (1.22 g, 7.5 mmol) in DMF (3.5 mL) was added dropwise for 10 min at rt and stirred the mixture at 60° C. for 2 h. Then, a solution of sodium methoxide (1 g, 18.6 mmol) in methanol (10 mL) was added dropwise at rt and stirring was continued for 2 h at 60° C. The mixture was allowed to rt and poured into cold water and stirred for 15 min. The solution was extracted with chloroform (3×100 mL) and the combined chloroform layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel using hexane-ethyl acetate (92:8) as eluent to give the product as a pale yellow color solid (1.1 g, 50%), mp 130-132° C. 1H NMR (400 MHz, DMSO-d6): δ 7.62-7.65 (2H, m), 7.38-7.48 (3H, m), 7.00 (1H, s), 4.29 (2H, br s), 3.74 (3H, s); LC-MS (positive ion mode): m/z 234 (M+H)+.

المصدر

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