1,2-Dimethoxyethane → (4-Hydroxy-3,5-dimethylphenyl)acetic acid

HRID 271148Notes

Reaction equation

HRID 271148 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4](CC#N)[CH:5]=[C:6]([CH3:9])[C:7]=1[OH:8].CO[CH2:15][CH2:16][O:17]C.[OH-:19].[K+]>O>[CH3:1][C:2]1[CH:3]=[C:4]([CH2:15][C:16]([OH:17])=[O:19])[CH:5]=[C:6]([CH3:9])[C:7]=1[OH:8]

Participants

5

Procedure

A suspension of (3,5-dimethyl-4-hydroxy-phenyl)-acetonitrile (4a) (550 mg, 0.003 mol) in water (0.98 mL) was treated with ethylene glycol dimethyl ether (6.6 mL, 0.063 mol) followed by potassium hydroxide (1.34 g, 0.024 mol). The reaction mixture was heated to reflux for 2 d. The reaction mixture was concentrated under vacuum. The resulting solid was diluted with water (100 mL) and extracted with ethyl acetate (2×75 mL). The organic layers were discarded. The aqueous layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution and was extracted with ethyl acetate (2×100 mL). The organic layers were combined, washed with a saturated aqueous sodium chloride solution (2×50 mL), dried with magnesium sulfate, filtered and concentrated under vacuum. The solid was purified by column chromatography using silica gel eluted with 15-25% ethyl acetate in petroleum ether to afford (3,5-dimethyl-4-hydroxy-phenyl)-acetic acid (5a) (30 mg, 5%) as a yellow solid; EI(+)-HRMS m/z calcd for C10H12O3 (M+) 180.0786, found 180.0782. Molecular Weight=180.2053; Exact Mass=180.0786

Workup

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 2 d
  3. concentrationThe reaction mixture was concentrated under vacuum
  4. additionThe resulting solid was diluted with water (100 mL)
  5. extractionextracted with ethyl acetate (2×75 mL)
  6. additionThe aqueous layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution
  7. extractionwas extracted with ethyl acetate (2×100 mL)
  8. washwashed with a saturated aqueous sodium chloride solution (2×50 mL)
  9. dry with materialdried with magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated under vacuum
  12. customThe solid was purified by column chromatography
  13. washeluted with 15-25% ethyl acetate in petroleum ether

Sources & evidence

ORD record
ord-5816bf481d8544a5ad1fd16863d54428
Source dataset
uspto-grants-2008_11
Patent number
US07452882B2

Reaction notes

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