Reacción #1994299

ord-cf80825d026045cd9ff24367d84a8c77

Ecuación de reacción

CCOC(=O)C(=O)CC(=O)/C=C/c1ccc(Cl)cc1
(E)-6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoic acid ethyl ester
CCOC(=O)C(=O)CC(=O)/C=C/c1ccc(Cl)cc1
(E)-6-(4-Chlorophenyl)-2,4-dioxo-hex-5-enoic acid ethyl ester
O=S(=O)(O)O
H2SO4
COC(=O)C(=O)CC(=O)/C=C/c1ccc(Cl)cc1
(E)-6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoic acid methyl ester

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaUpon cooling
  2. 2
    Concentraciónsolvent concentration, (E)-6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoic acid methyl ester (6; 22.7 g, 71%)
  3. 3
    Otrowas collected as yellow crystals

Procedimiento

A solution of (E)-6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoic acid ethyl ester (4; 33.39 g, 0.12 mol) and conc H2SO4 (0.5 mL) was stirred at reflux for 6 h in methyl alcohol (MeOH, 400 mL). Upon cooling and solvent concentration, (E)-6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoic acid methyl ester (6; 22.7 g, 71%) was collected as yellow crystals: mp 135-136° C.; 1H NMR (400 MHz, CDCl3) δ 14.74 (s, 1H), 7.67 (d, J=15.9 Hz, 1H), 7.49 (d, J=8.5 Hz, 2H), 7.38 (d, J=8.5 Hz, 2H), 6.61 (d, J=15.9 Hz, 1H), 6.53 (s, 1H), 3.92 (s, 3H); HRMS-ESI (m/z): calcd for C13H1ClO4, 266.034. found, 266.034.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08598086B2uspto-grants-2013_12