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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719908Generated: October 30, 2026

Water → 1-(t-Butyldimethylsilyl)-3-acetyl-4-(2'-hydroxyethyl)-2-azetidinone

https://huagongshe.com/reaction/1719908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ChlorideHCID 5234—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-(t-butyldimethylsilyl)-4-(2-acetoxyethyl)azetidin-2-oneHCID 13051149—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(t-Butyldimethylsilyl)-3-acetyl-4-(2'-hydroxyethyl)-2-azetidinoneHCID 14329000—

Reaction Steps

To a solution of 1.1 equivalents of freshly prepared lithium diisopropylamide in 3 ml anhydrous tetrahydrofuran under a nitrogen atmosphere at -78° is added a solution of 1-(t-butyldimethylsilyl)-4-(2'-acetoxyethyl)-2-azetidinone (61 mg, 0.225 mmole) in 1 ml anhydrous tetrahydrofuran which has been cooled to -78°. After 12 minutes the reaction mixture is poured into 5 ml water. The solution is saturated with sodium chloride and extracted with methylene chloride. The combined methylene chloride solutions are washed with brine, dried over magnesium sulfate and filtered. Evaporation of the filtrate under reduced pressure gives 50 mg of crude product. Purfication by preparative thick-layer chromatography on silica gel developing with ethyl acetate gives 1-(t-butyldimethylsilyl)-3-acetyl-4-(2'-hydroxyethyl)-2-azetidinone (19 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04543257
Source datasetuspto-grants-1985_09
ORD IDord-5744ca7b839f4fe6b9a338aff9682234
Source noteuspto-grants-1985_09