تفاعل #58985

ord-88340d42c4b64b29a8c104fdb5ee4786

معادلة التفاعل

Cl
hydrochloric acid
O=Cc1snnc1-c1ccc(F)cc1
4-(4-fluorophenyl)-1,2,3-thiadiazole-5-carbaldehyde
CCOC(=O)CP(=O)(OCC)OCC
ethyl diethylphosphonoacetate
[H-].[Na+]
sodium hydride
O=C(O)/C=C/c1snnc1-c1ccc(F)cc1
(2E)-3-[4-(4-fluorophenyl)-1,2,3-thiadiazol-5-yl]acrylic acid
المردود 60.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe mixture was extracted with ethyl acetate
  2. 2
    تركيزThe ethyl acetate layer was concentrated
  3. 3
    workup.ADDITIONa 6N aqueous hydrochloric acid solution (3 ml) and acetic acid (3 ml) were added to the residue
  4. 4
    workup.STIRRINGThe mixture was stirred for 3 hrs
  5. 5
    درجة الحرارةwith heating
  6. 6
    درجة الحرارةunder reflux
  7. 7
    تركيزThe reaction mixture was concentrated
  8. 8
    workup.ADDITIONpoured into water
  9. 9
    ترشيحThe precipitated solids were collected by filtration
  10. 10
    غسيلwashed with water
  11. 11
    أخرىdried

الإجراء التجريبي

A mixture of 4-(4-fluorophenyl)-1,2,3-thiadiazole-5-carbaldehyde (180 mg), ethyl diethylphosphonoacetate (450 mg), sodium hydride (60% in oil, 40 mg) and N,N-dimethylformamide (3 ml) was stirred at room temperature for 2 hrs. The reaction mixture was poured into a 1N aqueous hydrochloric acid solution and the mixture was extracted with ethyl acetate. The ethyl acetate layer was concentrated, and a 6N aqueous hydrochloric acid solution (3 ml) and acetic acid (3 ml) were added to the residue. The mixture was stirred for 3 hrs. with heating under reflux. The reaction mixture was concentrated and poured into water. The precipitated solids were collected by filtration, washed with water and dried to give (2E)-3-[4-(4-fluorophenyl)-1,2,3-thiadiazol-5-yl]acrylic acid (130 mg, yield 60%) as a pale-yellow solid.

المصدر

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