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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013833Generated: October 31, 2026

Dimethyl Sulfide → (R)-4-((R)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-4-oxo-butyraldehyde

https://huagongshe.com/reaction/1013833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantOzoneHCID 24823—
Reactant(R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-oneHCID 57671399—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(R)-4-((R)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-(3,5-dichloro-4'-fluoro-biphenyl-4-ylmethyl)-4-oxo-butyraldehydeHCID 57671350—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve (R)-4-Benzyl-3-[(S)-2-(3,5-dichloro-4′-fluoro-biphenyl-4-ylmethyl)-pent-4-enoyl]-oxazolidin-2-one (1.95 mmoles; 1.00 g) in dichloromethane (10 ml) and methanol (1 mL). Cool the mixture to −78° C. in a dry ice acetone bath and add ozone subsurface to the reaction with an exotherm to −71° C. The reaction turns blue, and then sweep with nitrogen to a clear color. Add dimethyl sulfide (2 mL; 27.20 mmoles) dropwise at −78° C. Warm the solution to ambient temperature and then test with KI starch paper (test is negative). Remove the solvents under vacuum, extract with MTBE, wash with pH=7 buffer, water, and brine. Concentrate the organics under vacuum to give a white non-crystalline solid (0.81 g). LCMS (M+1=515.39).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981918B2
Source datasetuspto-grants-2011_07
ORD IDord-89e1a09db3e344e2b38cfa7c89e9f50c
Source noteuspto-grants-2011_07