تفاعل #52302

ord-b1d78607255e4db591db91c514e39db9

معادلة التفاعل

O=Cc1ccc2c(c1)OCO2
piperonal
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
BrC(Br)(Br)Br
carbontetrabromide
BrC(Br)=Cc1ccc2c(c1)OCO2
title compound
المردود 74.0%
BrC(Br)=Cc1ccc2c(c1)OCO2
5-(2,2-Dibromo-vinyl)-benzo[1,3]dioxole
المردود 74.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    أخرىthe ice-water bath was removed
  3. 3
    أخرىquenched with saturated NaHCO3
  4. 4
    أخرىAqueous was separated
  5. 5
    استخلاصextracted with dichloromethane (2 times)
  6. 6
    تجفيفdried over Na2SO4
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated
  9. 9
    أخرىto give a redish colored residue, that
  10. 10
    ترشيحwas filtered through a short path silica gel plug
  11. 11
    غسيلeluting with DCM/hexane (10% to 20%)

الإجراء التجريبي

To a solution of piperonal (4.5 g, 30 mmol) and triphenylphosphine (24 g, 90 mmol) in DCM (120 mL) in an ice-water bath was added a solution of carbontetrabromide (15 g, 45 mmol) over a 10 minutes period. After the addition completed, the ice-water bath was removed, the reaction stirred at ambient temperature for 2 h, and then quenched with saturated NaHCO3. Aqueous was separated, and extracted with dichloromethane (2 times). The organic layers were combined, dried over Na2SO4, filtered, and concentrated to give a redish colored residue, that was filtered through a short path silica gel plug, eluting with DCM/hexane (10% to 20%). Concentration of the filtrate gave the title compound (6.5 g, 74% yield) as a pale yellow liquid. 1H NMR (CDCl3) δ 7.36 (s, 1H), 7.18 (d, 1H, J=1.6 Hz), 6.95 (dd, 1H, J=1.5, 8.1 Hz), 6.79 (d, 1H, J=8.1 Hz), 5.99 (s, 2H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06855722B2uspto-grants-2005_02