Réaction #2286286

ord-1e3a61743cef421184ade6821d55e122

Équation de réaction

Cc1cc(CC(=O)O)cc(Cl)c1O
(3-chloro-4-hydroxy-5-methyl-phenyl)-acetic acid
Cc1cc(CC(=O)O)cc(Cl)c1O
(3-Chloro-4-hydroxy-5-methyl-phenyl)-acetic acid
O=S(=O)(O)O
sulfuric acid
CO
methanol
COC(=O)Cc1cc(C)c(O)c(Cl)c1
acetic acid methyl ester
Rendement 91.0%
COC(=O)Cc1cc(C)c(O)c(Cl)c1
(3-Chloro-4-hydroxy-5-methyl-phenyl)-acetic acid methyl ester
Rendement 91.0%

Conditions de réaction

Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ConcentrationAt this time, the reaction mixture was concentrated under vacuum
  2. 2
    workup.ADDITIONThe resulting oil was diluted with ethyl acetate (100 mL)
  3. 3
    LavageThe organics were washed with water (2×50 mL)
  4. 4
    Séchagedried with magnesium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    Concentrationconcentrated
  7. 7
    AutreThe resulting residue was purified by column chromatography
  8. 8
    Lavageeluted with 10% ethyl acetate in petroleum ether

Mode opératoire

A solution of (3-chloro-4-hydroxy-5-methyl-phenyl)-acetic acid (5b) (1.4 g, 6.98 mmol) in methanol (60 mL) was treated with concentrated sulfuric acid (0.5 mL) at room temperature under argon. The reaction mixture was heated to 70° C. for 24 h. At this time, the reaction mixture was concentrated under vacuum. The resulting oil was diluted with ethyl acetate (100 mL). The organics were washed with water (2×50 mL), dried with magnesium sulfate, filtered and concentrated. The resulting residue was purified by column chromatography using silica gel eluted with 10% ethyl acetate in petroleum ether to afford 3-chloro-4-hydroxy-5-methyl-phenyl)-acetic acid methyl ester (6b) (1.36 g, 91%) as a white solid; EI(+)-HRMS m/z calcd for C10H11ClO3 (M+) 214.0397, found 214.0400. Molecular Weight=214.6504; Exact Mass=214.0397

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE046024E1uspto-grants-2016_06