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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543560Generated: November 1, 2026

Triethylamine → 1-[tert-Butyl(dimethyl)silyl]-4-(prop-2-en-1-yl)azetidin-2-one

https://huagongshe.com/reaction/543560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantAllylazetidinoneHCID 12376723—
ReactantWater ethylacetateHCID 22728543—
SolventDimethylformamideHCID 6228—
Product1-[tert-Butyl(dimethyl)silyl]-4-(prop-2-en-1-yl)azetidin-2-oneHCID 12882104—

Reaction Steps

Allylazetidinone (0.22 g) was dissolved in dry N,N-dimethylformamide (5 ml) containing t-butyldimethylsilyl chloride (0.33 g). The solution was cooled to 0° and was treated with triethylamine (0.22 g) in N,N-dimethylformamide (1 ml) over a period of 15 minutes. After a further 15 minutes the solution was poured into ethylacetate/water. The organic phase was separated, washed with dil HCl, brine, dried (Na2SO4), evaporated, and chromatographed on silica gel 60 (230 mesh) eluting with ethylacetate. This gave 4-allyl-1-t-butyldimethylsilylazetidin-2-one (0.39 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04446146
Source datasetuspto-grants-1984_05
ORD IDord-097052cf6dbe476c9929959513933e1f
Source noteuspto-grants-1984_05