Реакция #2286286

ord-1e3a61743cef421184ade6821d55e122

Уравнение реакции

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
Выход 91.0%
COC(=O)Cc1cc(C)c(O)c(Cl)c1
(3-Chloro-4-hydroxy-5-methyl-phenyl)-acetic acid methyl ester
Выход 91.0%

Условия реакции

Температура
70°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеAt this time, the reaction mixture was concentrated under vacuum
  2. 2
    workup.ADDITIONThe resulting oil was diluted with ethyl acetate (100 mL)
  3. 3
    ПромывкаThe organics were washed with water (2×50 mL)
  4. 4
    Сушкаdried with magnesium sulfate
  5. 5
    Фильтрацияfiltered
  6. 6
    Концентрированиеconcentrated
  7. 7
    ДругоеThe resulting residue was purified by column chromatography
  8. 8
    Промывкаeluted with 10% ethyl acetate in petroleum ether

Методика

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

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE046024E1uspto-grants-2016_06