HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888205Generated: October 30, 2026
Methyl iodide → Diisopropyl (2R,3S)-2-hydroxy-3-methylsuccinate
https://huagongshe.com/reaction/888205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Diisopropyl (S)-(-)-malate | HCID 11333435 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diisopropyl (2R,3S)-2-hydroxy-3-methylsuccinate | HCID 58488018 | — |
Reaction Steps
To a cold (−78° C.) solution of diisopropyl-(S)-(−)-malate (4.72 mL, 22.9 mmol, 1 eq.) in anhydrous THF (8.50 mL) was added slowly a solution (1 M) of lithium bis(trimethylsilyl)amide (48.1 mL, 48.1 mmol, 2.10 eq.) in THF. The temperature was raised to 20° C. over 30 minutes, than lowered again to −78° C. Iodomethane (1.7 mL, 28 mmol, 1.20 eq.) was added and the mixture stirred at RT for 16 hours. The reaction mixture was then cooled to 0° C. and a saturated solution of NH4Cl was added. The resulting mixture was diluted with water, extracted three times with EtOAc. The combined organic phases were washed with brine, dried over MgSO4, filtered and evaporated under reduced pressure. The residue was then purified by chromatography (SiO2, 20/80 EtOAc/c-hex) to give the product (mixture of diatereoisomers) as a colourless oil (3.77 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08247437B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-74e584a170694903a647c786b6e3f8b4 |
|---|
| Source note | uspto-grants-2012_08 |
|---|