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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290994Generated: October 31, 2026

Triethylamine → HCID 56634697, compound

https://huagongshe.com/reaction/2290994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 56610278HCID 56610278—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 56634697HCID 56634697—

Reaction Steps

A solution, cooled to 0°, of 17.1 g (0.1 mmol) of (S)-4-[(R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-azetidinone and 15.1 g (0.1 mol of t-butyldimethylchlorosilane in 100 ml of dimethylformamide is treated while stirring with 10.6 g (0.105 mol) of triethylamine, whereby a precipitate results immediately. The mixture is stirred at 0° for 2 hours, then diluted with 200 ml of ether and the reaction mixture is washed five times with 80 ml of water each time. The aqueous phases are then extracted with 100 ml of ether. The organic phases are dried over sodium sulphate and evaporated, whereupon the residual oil is distilled. There is obtained (S)-1-(t-butyldimethylsilyl)-4-[(R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-azetidinone of boiling point 84°-87° (0.5 Torr); [α]D20 =-22.7° (c=1, ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04619787
Source datasetuspto-grants-1986_10
ORD IDord-3fd5e45070b54a458fa37368d54f250f
Source noteuspto-grants-1986_10