Isopropylamine → 2-(4-chlorophenyl)-2-hydroxypropanoic acid

Temperature

90 °C

MCPBA (35 g, 77%, 156 mmol) was added to a solution of methyl 2-(4-chlorophenyl)-acrylate (20 g, 102 mmol) in CHCl3 (200 mL). The mixture was refluxed for 24 hours. The reaction was cooled to room temperature, diluted with chloroform (200 mL) and washed with 10% Na2S2O3, 10% NaHCO3 and water. The organic phase was dried and concentrated. The residue was subject to column chromatography, eluted by hexane/ethyl acetate (9:1) to give methyl 2-(4-chlorophenyl)oxirane-2-carboxylate. Methyl 2-(4-chlorophenyl)oxirane-2-carboxylate (2 g, 9.4 mmol) and ethanol (10 mL) and isopropylamine (1 mL, 11.7 mmol) were added to a 50 mL high pressure bomb. The mixture was heated to 90° C. for 12 hours in the bomb. After cooling, the solvent was removed, and the residue was dissolved in DCM (20 mL) and TEA (2 mL). (Boc)2O (4 g, 23.0 mmol) was added to it. The mixture was stirred at room temperature for 48 hours. The solvent was removed, and the residue was dissolved in THF (20 mL). LiOH (3M, 14 mL) was added to the mixture. The mixture was stirred at room temperature for 16 hours and refluxed for 2 hours. After cooling, the mixture was quenched with 2N HCl (21 mL). The solvent was removed and the residue was subject to column chromatography, eluted by hexane/ethyl acetate (1:1) to give 3-(tert-butoxycarbonykisopropyl)amino)-2-(4-chlorophenyl)-2-hydroxypropanoic acid. LCMS (APCI+) [M−Boc+H]+ 258.1; Rf: 3.66 min.

1. temperatureAfter cooling
2. customthe solvent was removed
3. dissolutionthe residue was dissolved in DCM (20 mL)
4. customThe solvent was removed
5. dissolutionthe residue was dissolved in THF (20 mL)
6. additionLiOH (3M, 14 mL) was added to the mixture
7. stirringThe mixture was stirred at room temperature for 16 hours
8. temperaturerefluxed for 2 hours
9. temperatureAfter cooling
10. customthe mixture was quenched with 2N HCl (21 mL)
11. customThe solvent was removed
12. washeluted by hexane/ethyl acetate (1:1)

ORD record

ord-cf9cebef7fe54101a474c2d832d19c09

Source dataset

uspto-grants-2016_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09359340B2