Sulfuric Acid → (R)-2-Hydroxy-3-(4-methoxy-phenyl)-propionic acid ethyl ester

Commercially available O-methyl-D-tyrosine (5.00 g) was dissolved in 1,4-dioxane (62.5 ml), and thereto were added successively dropwise an aqueous sulfuric acid solution (5.4 g/17.5 ml of water) and an aqueous sodium nitrite solution (6.3 g/15.0 ml of water) under ice-cooling, and the mixture was stirred at room temperature. Ten hours later, to the reaction solution was added a saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over sodium hydrogen sulfate, filtered, and concentrated under reduced pressure. The resultant was duly dried, and then, the obtained residue was dissolved in ethanol (50 ml), and further thereto was added conc. sulfuric acid (200 μL). The mixture was refluxed for 15 hours, and the reaction solution was added dropwise into ice-water (50 ml), and the mixture was extracted with ethyl acetate (50 ml). The organic layer was washed successively with a saturated aqueous sodium hydrogen carbonate solution and a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (the developing solvent: hexane/ethyl acetate=5/1) to give the title compound (3.40 g) as a colorless liquid.

1. extractionthe mixture was extracted with ethyl acetate
2. washThe organic layer was washed with a saturated aqueous sodium chloride solution
3. dry with materialdried over sodium hydrogen sulfate
4. filtrationfiltered
5. concentrationconcentrated under reduced pressure
6. customThe resultant was duly dried
7. dissolutionthe obtained residue was dissolved in ethanol (50 ml)
8. additionfurther thereto was added conc. sulfuric acid (200 μL)
9. temperatureThe mixture was refluxed for 15 hours
10. additionthe reaction solution was added dropwise into ice-water (50 ml)
11. extractionthe mixture was extracted with ethyl acetate (50 ml)
12. washThe organic layer was washed successively with a saturated aqueous sodium hydrogen carbonate solution
13. dry with materiala saturated aqueous sodium chloride solution, dried over sodium sulfate
14. filtrationfiltered
15. concentrationconcentrated under reduced pressure
16. customThe obtained residue was purified by silica gel column chromatography (the developing solvent

ORD record

ord-f95f0cd06f084ed694df7e543025003c

Source dataset

uspto-grants-2013_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08389511B2