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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantDiisopropyl (S)-(-)-malateHCID 11333435—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductDiisopropyl (2R,3S)-2-hydroxy-3-methylsuccinateHCID 58488018—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247437B2
Source datasetuspto-grants-2012_08
ORD IDord-74e584a170694903a647c786b6e3f8b4
Source noteuspto-grants-2012_08