Potassium Hydroxide → (2S,3R)-2-hydroxy-3-methylbutanedioic acid

Temperature

0 °C

Diisopropyl (2S,3R)-2-hydroxy-3-methylsuccinate (3.70 g; 15.93 mmol; 1.0 eq.) was taken in THF (55 mL), cooled to 0° C. and treated with KOH (5.36 g, 96 mmol) in water (18.5 mL). The resulting mixture was stirred at RT for 48 h. THF was removed and the residue was taken in water. The aqueous layer was washed with Et2O (100 mL) and was acidified with an aqueous solution of HCl (1.5 N), then was extracted with EtOAc (continuous extraction during 20 hours). The organic phase was dried over Na2SO4 and then concentrated to give the title product (mixture of diastereoisomers) as pale yellow oil (2.4 g, quant.).

1. customTHF was removed
2. washThe aqueous layer was washed with Et2O (100 mL)
3. extractionwas extracted with EtOAc (continuous extraction during 20 hours)
4. dry with materialThe organic phase was dried over Na2SO4
5. concentrationconcentrated

ORD record

ord-c26e2230352442f0a2db2902701c403c

Source dataset

uspto-grants-2011_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08008302B2