Reacción #1382672

ord-4b7d4f1e09594a07a76c3ab10e97afc9

Ecuación de reacción

COC1(OC)C(Cl)=C(Cl)C(Cl)=C1Cl
5,5-dimethoxy-1,2,3,4-tetrachlorocyclopentadiene
O=c1occo1
vinylene carbonate
COC1(OC)C2(Cl)C(Cl)=C(Cl)C1(Cl)C1OC(=O)OC12
solid
Rendimiento 94.5%
COC1(OC)C2(Cl)C(Cl)=C(Cl)C1(Cl)C1OC(=O)OC12
1,7,8,9-Tetrachloro-10,10-dimethoxy-3,5-dioxa-tricyclo[5.2.1.02,6]dec-8-en-4-one
Rendimiento 94.5%

Condiciones de reacción

Temperatura
90°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroIn a 500 mL 3N RB flask equipped with a water condenser, N2 flow adapter
  2. 2
    Temperaturaupon cooling
  3. 3
    Otrowas recrystallized from THF
  4. 4
    Filtraciónfiltered

Procedimiento

In a 500 mL 3N RB flask equipped with a water condenser, N2 flow adapter and thermometer, was placed 5,5-dimethoxy-1,2,3,4-tetrachlorocyclopentadiene (20.7 g, 0.078 mol) and vinylene carbonate (6.7 g, 0.078 mol). The mixture was heated to 90° C. for 4 h, then at 60° C. for 63 h. The reaction was judged complete by TLC and upon cooling, the product solidified, was recrystallized from THF and filtered to provide a white solid (25.80 g, 94%). (TLC 20% EtOAc/hexanes Rf 0.29); 1H NMR (400 MHz, CDCl3) δ 5.13 (s, 2H), 3.59 (s, 3H), 3.56 (s, 3H); GCMS m/z 348 (M)+; mp 160–162° C.; Anal. Calcd. for C10H8Cl4O5: C, 34.32; H, 2.30. Found C, 34.32; H, 2.27.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07241887B2uspto-grants-2007_07