Réaction #2286285

ord-3e3311f0edeb4d86921a3b59d9703971

Équation de réaction

Cc1cc(CC#N)cc(Cl)c1O
(3-chloro-4-hydroxy-5-methyl-phenyl)-acetonitrile
Cc1cc(CC#N)cc(Cl)c1O
(3-Chloro-4-hydroxy-5-methyl-phenyl)-acetonitrile
COCCOC
ethylene glycol dimethyl ether
[K+].[OH-]
potassium hydroxide
Cc1cc(CC(=O)O)cc(Cl)c1O
(3-chloro-4-hydroxy-5-methyl-phenyl)-acetic acid
Rendement 98.3%
Cc1cc(CC(=O)O)cc(Cl)c1O
(3-Chloro-4-hydroxy-5-methyl-phenyl)-acetic acid
Rendement 98.3%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction mixture was heated
  2. 2
    Températureto reflux for 24 h
  3. 3
    ConcentrationAt this time, the reaction mixture was concentrated under vacuum
  4. 4
    workup.ADDITIONThe resulting solid was diluted with water (100 mL)
  5. 5
    Extractionextracted with ethyl acetate (2×50 mL)
  6. 6
    workup.ADDITIONThe water layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution
  7. 7
    Extractionwas extracted with ethyl acetate (2×50 mL)
  8. 8
    Lavagewashed with a saturated aqueous sodium chloride solution (50 mL)
  9. 9
    Séchagedried with magnesium sulfate
  10. 10
    Filtrationfiltered
  11. 11
    Concentrationconcentrated under vacuum
  12. 12
    AutreThe resulting solid was dried under high vacuum overnight

Mode opératoire

A suspension of (3-chloro-4-hydroxy-5-methyl-phenyl)-acetonitrile (4b) (1.3 g, 0.0071 mol) in water (2.06 mL) was treated with ethylene glycol dimethyl ether (13.93 mL, 0.133 mol) followed by potassium hydroxide (2.8 g, 0.0071 mol). The reaction mixture was heated to reflux for 24 h. At this time, the reaction mixture was concentrated under vacuum. The resulting solid was diluted with water (100 mL) and extracted with ethyl acetate (2×50 mL). The organic layers were discarded. The water layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution and was extracted with ethyl acetate (2×50 mL). The organic layers were combined, washed with a saturated aqueous sodium chloride solution (50 mL), dried with magnesium sulfate, filtered and concentrated under vacuum. The resulting solid was dried under high vacuum overnight to afford (3-chloro-4-hydroxy-5-methyl-phenyl)-acetic acid (5b) (1.4 g, 97%) as a white solid; EI(+)-HRMS m/z calcd for C9H9ClO3 (M+) 200.0240, found 200.0247. Molecular Weight=200.6233; Exact Mass=200.0240

Source

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