تفاعل #2254202

ord-8317d059fb864abfb2301d43accd254c

معادلة التفاعل

Fc1cc[c]([Mg][Br])cc1
p-fluorophenylmagnesium bromide
COC(=O)C(C#N)=C1CCOCC1
Methyl 2-cyano-2-(oxan-4-ylidene)acetate
COC(=O)C(C#N)C1(c2ccc(F)cc2)CCOCC1
methyl 2-cyano-2-[4-(4-fluorophenyl)oxan-4-yl]acetate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA round bottom flask was equipped with a condenser, addition funnel
  2. 2
    درجة الحرارةwhile cooling the reaction flask in an ice bath
  3. 3
    استخلاصThe product was extracted with Et2O (3×50 ml)
  4. 4
    غسيلwashed with brine (50 ml)
  5. 5
    أخرىdried (NA2SO4)
  6. 6
    تركيزconcentrated
  7. 7
    أخرىPurified by normal phase SiO2 chromatography (7% to 60% EtOAc/hexanes)

الإجراء التجريبي

A round bottom flask was equipped with a condenser, addition funnel and rubber septum with nitrogen inlet was charged with a solution of p-fluorophenylmagnesium bromide (2.0 M in diethyl ether, 1.99 ml, 3.97 mmol) and CuI (63 mg, 0.331 mmol) in 10 ml dry diethyl ether (10 ml). Methyl 2-cyano-2-(oxan-4-ylidene)acetate (600 mg, 3.31 mmol) in diethyl ether (10 ml) was added drop-wise over 30 min while cooling the reaction flask in an ice bath. The mixture was then stirred for 3 h. The reaction mixture was poured into a 50 g ice/1 N HCl (25 ml) mixture. The product was extracted with Et2O (3×50 ml), washed with brine (50 ml), dried (NA2SO4) and concentrated. Purified by normal phase SiO2 chromatography (7% to 60% EtOAc/hexanes) to give methyl 2-cyano-2-[4-(4-fluorophenyl)oxan-4-yl]acetate as a white solid (730 mg, 80%, m/z: 277.1 [M+Na]+ observed).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09044469B2uspto-grants-2015_06