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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867578Generated: October 30, 2026

Pyridine → 1-(t-Butyldimethylsilyl)-4-(2-oxoethyl)-2-azetidinone

https://huagongshe.com/reaction/867578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-(t-butyldimethylsilyl)-4-(2-hydroxyethyl)-azetidin-2-oneHCID 13104623—
SolventDichloromethaneHCID 6344—
Product1-(t-Butyldimethylsilyl)-4-(2-oxoethyl)-2-azetidinoneHCID 1280471874%

Reaction Steps

Anhydrous CrO3 (1.94 g, 19.38 mmol) is added to a solution of anhydrous pyridine (3.07 g, 38.76 mmol) in anhydrous CH2Cl2 (50 ml). The resulting mixture is stirred at r.t. for 15 min. A solution of 1-(t-butyldimethylsilyl)-4-(2-hydroxyethyl)-2-azetidinone (0.74 g, 3.23 mmol) in anhydrous CH2Cl2 5 ml is added all at once. After stirring for 5 min, the CH2Cl2 solution is separated from a dark gummy precipitate which is washed with more CH2Cl2. The combined CH2Cl2 solution is evaporated under vacuum. The residue is taken up in ether filtered and washed with 5% NaHCO3, 5% HCl, 5%NaHCO3 and brine then dried and evaporated to give the aldehyde (0.543 g 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775669
Source datasetuspto-grants-1988_10
ORD IDord-c3117c64dfc14b3398e333b21e7a11d6
Source noteuspto-grants-1988_10