HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677765Generated: October 31, 2026
Potassium Hydroxide → (2S,3R)-2-hydroxy-3-methylbutanedioic acid
https://huagongshe.com/reaction/1677765
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diisopropyl (2S,3R)-2-hydroxy-3-methylsuccinate | HCID 58487994 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S,3R)-2-hydroxy-3-methylbutanedioic acid | HCID 14325352 | — |
Reaction Steps
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.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008302B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-c26e2230352442f0a2db2902701c403c |
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| Source note | uspto-grants-2011_08 |
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