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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920228Generated: October 30, 2026

Water → HCID 59226578, compound

https://huagongshe.com/reaction/1920228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium periodateHCID 23667635—
Reactant(4R)-4-(benzyloxymethyl)-5-(but-3-en-2-yl)oxazolidin-2-oneHCID 59226487—
CatalystOsmium TetroxideHCID 30318—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 59226578HCID 59226578—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (4R)-4-(benzyloxymethyl)-5-(but-3-en-2-yl)oxazolidin-2-one (1.0 equiv.) in 2:1 MeOH/H2O (0.04 M) was added osmium tetroxide 4% in H2O (0.07 equiv) and sodium periodate (3.0 equiv.). After stirring for 3 hours, the white precipitate was filtered and rinsed with EtOAc. The combined filtrate was concentrated in vacuo and the residue was dissolved in EtOAc, washed with NaCl(sat.), dried over MgSO4, filtered and concentrated. The crude aldehyde was dissolved in EtOH (0.08 M) and upon cooling to 0° C., sodium borohydride (2.0 equiv.) was added. After stirring for 15 hours and coming to room temperature the reaction was quenched by addition of H2O. After stirring for 20 minutes, the EtOH was removed in vacuo, EtOAc was added and the solution was washed with 1N HCl, NaHCO3(sat.) and NaCl(sat.), dried over MgSO4, filtered and concentrated yielding after purification by silica gel chromatography (4R)-4-(benzyloxymethyl)-5-(1-hydroxypropan-2-yl)oxazolidin-2-one as a 3:1 mixture of isomers (60%). LCMS (m/z): 266.1 (MH+); LC Rt=2.28 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168794B2
Source datasetuspto-grants-2012_05
ORD IDord-eaef5fd2975f473f811a9a5ff070c783
Source noteuspto-grants-2012_05