Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591270Generated: October 31, 2026

Pyridine → tert-Butyl (S)-2-((tert-butoxycarbonyl)amino)-4-oxobutanoate

https://huagongshe.com/reaction/591270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant(S)-tert-Butyl 2-((tert-butoxycarbonyl)amino)-4-hydroxybutanoateHCID 11054918—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl (S)-2-((tert-butoxycarbonyl)amino)-4-oxobutanoateHCID 1090176299.7%

Reaction Steps

To a solution of 1.10 g (4.0 mmol) tert-butyl N-(tert-butoxycarbonyl)-L-homoserinate (prepared according to J. Org. Chem. 1988, 53, 1900-1903) in dichloromethane (50 mL) was added pyridine (0.97 mL, 12.0 mmol), followed by 2.55 g Dess Martin periodinane (6.0 mmol), at room temperature. The mixture was stirred 90 min at room temperature prior to being diluted with ethyl acetate (40 mL). The mixture was washed with 10% aqueous sodium thiosulfate, saturated aqueous sodium bicarbonate and brine. The organic layer was dried over sodium sulfate and then evaporated. The crude product (1.09 g, quantitative yield) was used immediately without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238631B2
Source datasetuspto-grants-2016_01
ORD IDord-27212c75d7a44312ab293cd2fdf0abdc
Source noteuspto-grants-2016_01