تفاعل #1271853

ord-94d263307dc946c2a1c1579f0dcc760a

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe mixture was stirred for 2 hours during which time it
  2. 2
    درجة الحرارةto warm to room temperature
  3. 3
    استخلاصextracted with ethyl acetate (3×250 mL)
  4. 4
    غسيلThe combined organic extracts were then washed with brine
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىThe crude product was chromatographed over silica gel
  8. 8
    غسيلElution with ethyl acetate/hexanes (1:10)

الإجراء التجريبي

Triethyl phosphonoacetate (4.05 mL, 202 mmol) was added dropwise to a stirred suspension of sodium hydride (0.80 g, 20 mmol) in anhydrous tetrahydrofuran (20 mL) at 0° C. under nitrogen. The mixture was stirred at 0° C. for 20 minutes. A solution of 2,3-methylenedioxybenzaldehyde (2.50 g, 16.7 mmol) in tetrahydrofuran (10 mL) was added dropwise at 0° C. The mixture was stirred for 2 hours during which time it was allowed to warm to room temperature. The mixture was poured into water (250 mL), and extracted with ethyl acetate (3×250 mL). The combined organic extracts were then washed with brine, dried (MgSO4) and concentrated in vacuo. The crude product was chromatographed over silica gel. Elution with ethyl acetate/hexanes (1:10) gave ethyl 2,3-methylenedioxycinnamate as a colourless solid (3.50 g, 92%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08669280B2uspto-grants-2014_03