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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009103Generated: October 27, 2026

Pyridine → tert-butyl (2S,3S)-3-(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)-4-oxobutan-2-ylcarbamate

https://huagongshe.com/reaction/1009103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactanttert-Butyl (2S,3S)-3-(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)-4-hydroxybutan-2-ylcarbamateHCID 86614117—
SolventEthyl AcetateHCID 8857—
Producttert-butyl (2S,3S)-3-(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)-4-oxobutan-2-ylcarbamateHCID 86614118—

Reaction Conditions

Temperature23 °C

Reaction Steps

To a 150 mL RBF containing tert-butyl(2S,3S)-3-(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)-4-hydroxybutan-2-ylcarbamate (170.00 mg, 411 μmol) was added DCM (10 mL) and the mixture was allowed to stir at 23° C. for 2 minutes. At this time, pyridine (299 μl, 3699 μmol) was added via syringe before the addition of Dess-MartinPeriodinane (262 mg, 617 μmol) in one portion. The reaction stayed a clear solution and was allowed to stir 1 h before loading directly to a silica gel column (20% EtOAc). The purified product was concentrated to give the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973047B2
Source datasetuspto-grants-2011_07
ORD IDord-479263f6935342a79bc7081bea46c940
Source noteuspto-grants-2011_07