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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711062Generated: November 1, 2026

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

https://huagongshe.com/reaction/1711062

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 with 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 numberUS07790729B2
Source datasetuspto-grants-2010_09
ORD IDord-fb106b802a154c36b4c40c17ecacca97
Source noteuspto-grants-2010_09