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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098248Generated: October 26, 2026

Magnesium trifluoromethanesulfonate → (R)-methyl 2-hydroxy-3-((S)-1-(triisopropylsilyloxy)propan-2-yloxy)propanoate

https://huagongshe.com/reaction/1098248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMagnesium trifluoromethanesulfonateHCID 2734125—
ReactantMethyl (2R)-2-oxiranecarboxylateHCID 9877347—
Reactant(S)-1-(triisopropylsilyloxy)propan-2-olHCID 57504699—
SolventEthyl AcetateHCID 8857—
Product(R)-methyl 2-hydroxy-3-((S)-1-(triisopropylsilyloxy)propan-2-yloxy)propanoateHCID 8664084741.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Magnesium trifluoromethanesulfonate (1.263 g, 3.92 mmol) was added to a mixture of (S)-1-(triisopropylsilyloxy)propan-2-ol (4.55 g, 19.59 mmol) and (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) in ethyl acetate (40 mL). The resulting suspension was heated to 80° C. for 72 hours. Further (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) was added and the mixture stirred at 80° C. for 48 hrs. Further (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) was added and the mixture stirred for 24hrs. The mixture was allowed to cool, filtered through a bed of silica (˜10 g), washed through with EtOAc and evaporated. The crude product was purified by flash silica chromatography, elution gradient 10 to 50% EtOAc in isohexane, to afford the product (2.7 g, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143263B2
Source datasetuspto-grants-2012_03
ORD IDord-653a862f75c2436d96da5555cc93da7b
Source noteuspto-grants-2012_03