HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → D-Erythro-3-Methylmalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diisopropyl (2R,3S)-2-hydroxy-3-methylsuccinate | HCID 58488018 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | D-Erythro-3-Methylmalate | HCID 440892 | 40% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Diisopropyl (2R,3S)-2-hydroxy-3-methylsuccinate (9.75 g; 42.0 mmol; 1.00 eq.) was taken in THF (146 mL), cooled to 0° C. and was treated with KOH (14.1 g, 152 mmol) in water (49 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 ether (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 a pale yellow oil (2.49 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247437B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-470c4fdfd8784dbba0aed705d218b182 |
| Source note | uspto-grants-2012_08 |