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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500914Generated: November 2, 2026

tert-Butyldimethylsilyl chloride → tert-Butyl 3-(tert-butyldimethylsilyloxy)azetidine-1-carboxylate

https://huagongshe.com/reaction/500914

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-(tert-butyldimethylsilyloxy)azetidine-1-carboxylateHCID 5942459975.4%

Reaction Steps

A solution of tert-butyl 3-hydroxyazetidine-1-carboxylate (1 g, 5.77 mmol), TBSCl (6.35 mmol, 956 mg) in DCM (11.5 mL), was stirred for 72 hrs at room temperature. The solvent was removed under reduced pressure, EtOAc was added to the residue, and the solid material was removed by filtration. The filtrate was concentrated under reduced pressure and the residue was purified by flash chromatography with gradient elution wit EtOAc/hexane (9:1) to EtOAc/hexane (1:1), to afford title compound 295 (1.25 g, 75% yield) as a syrup. MS (m/z): 310.1 (M+23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772247B2
Source datasetuspto-grants-2010_08
ORD IDord-b4d3cbb5c2204937b42c5cab58e190eb
Source noteuspto-grants-2010_08