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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856068Generated: November 1, 2026

Benzyl acetate → N-(t-butyldimethylsilyl)-3-azido-4-(3-benzyloxycarbonyl 2-hydroxypropyl)-azetidin-2-one

https://huagongshe.com/reaction/1856068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl acetateHCID 8785—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-(t-butyldimethylsilyl)-3-azido-4-(2-oxoethyl)azetidin-2-oneHCID 20563653—
SolventTetrahydrofuranHCID 8028—
ProductN-(t-butyldimethylsilyl)-3-azido-4-(3-benzyloxycarbonyl 2-hydroxypropyl)-azetidin-2-oneHCID 20563667—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of benzyl acetate (0.011 mol) in anhydrous tetrahydrofuran (5 ml) is added dropwise to solution of lithium diisopropylamide (0.011 mol) in anhydrous tetrahydrofuran (20 ml) at -78° C. After stirring 15 more min at -78° C. the reaction mixture is treated dropwise with a solution of N-(t-butyldimethylsilyl)-3-azido-4-(2-oxoethyl)-azetidin-2-one (0.01 mol) in tetrahydrofuran (10 ml). The mixture is stirred at -78° an additional 15 min and then quenched with 2.5 N hydrochloric acid (10 ml). The mixture is diluted with ethyl acetate, washed with water, 5% sodium bicarbonate solution, and brine, dried with magnesium sulfate, and evaporated under vacuum to afford N-(t-butyldimethylsilyl)-3-azido-4-(3-benzyloxycarbonyl-2-hydroxypropyl)-azetidin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04217453
Source datasetuspto-grants-1980_08
ORD IDord-b9574fb81bf24a288529abb7e3172611
Source noteuspto-grants-1980_08