1,2-Dimethoxyethane → (3-Chloro-4-hydroxy-5-methyl-phenyl)-acetic acid

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

1. temperatureThe reaction mixture was heated
2. temperatureto reflux for 24 h
3. concentrationAt this time, the reaction mixture was concentrated under vacuum
4. additionThe resulting solid was diluted with water (100 mL)
5. extractionextracted with ethyl acetate (2×50 mL)
6. additionThe water layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution
7. extractionwas extracted with ethyl acetate (2×50 mL)
8. washwashed with a saturated aqueous sodium chloride solution (50 mL)
9. dry with materialdried with magnesium sulfate
10. filtrationfiltered
11. concentrationconcentrated under vacuum
12. customThe resulting solid was dried under high vacuum overnight

ORD record

ord-c8b168623f47424086e59bb7b6a2dd97

Source dataset

uspto-grants-2008_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07452882B2