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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098218Generated: October 27, 2026

Magnesium trifluoromethanesulfonate → (S)-Methyl 3-((S)-1-(tert-butyldimethylsilyloxy)propan-2-yloxy)-2-hydroxypropanoate

https://huagongshe.com/reaction/1098218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMagnesium trifluoromethanesulfonateHCID 2734125—
ReactantMethyl (2S)-2-oxiranecarboxylateHCID 10942355—
Reactant(S)-1-((Tert-butyldimethylsilyl)oxy)propan-2-OLHCID 13175136—
SolventEthyl AcetateHCID 8857—
Product(S)-Methyl 3-((S)-1-(tert-butyldimethylsilyloxy)propan-2-yloxy)-2-hydroxypropanoateHCID 8664084637.8%

Reaction Conditions

Temperature10 °C

Reaction Steps

Magnesium trifluoromethanesulfonate (0.974 g, 3.02 mmol) was added in one portion to (S)-methyl oxirane-2-carboxylate (1.234 g, 12.08 mmol) and (S)-1-(tert-butyldimethylsilyloxy)propan-2-ol (CAS no. 113534-13-7) (2.30 g, 12.08 mmol) in EtOAc (5 mL) cooled to 10° C. The resulting suspension was stirred at 10° C. for 10 minutes and then warmed to 45° C. and stirred for 2 days. The crude product was purified by flash silica chromatography, eluting with 0 to 30% EtOAc in isohexane to afford the product (1.336 g, 37.8%). 1H NMR (400 MHz, DMSO) δ0.00 (s, 6H), 0.83 (s, 9H), 0.98 (d, 3H), 3.34-3.53 (m, 3H), 3.55-3.64 (m, 5H), 4.11 (q, 1H), 5.39 (d, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143263B2
Source datasetuspto-grants-2012_03
ORD IDord-def69126da904439adb9a57acd51ca11
Source noteuspto-grants-2012_03