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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778427Generated: October 31, 2026

Imidazole → 3-((Tert-butyldiphenylsilyl)oxy)azetidine

https://huagongshe.com/reaction/1778427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant3-Hydroxyazetidine hydrochlorideHCID 2759290—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-((Tert-butyldiphenylsilyl)oxy)azetidineHCID 1784253182.5%

Reaction Steps

To a solution of azetidin-3-ol hydrochloride (5.11 g, 46.7 mmol, 1.0 equiv) and 1H-imidazole (9.52 g, 140 mmol, 3.0 equiv) in DCM (100 mL) at 0° C. was added TBDPSCl (19.18 g, 70 mmol, 1.5 equiv) dropwise. The resulting mixture was stirred at rt overnight and then diluted with water, and extracted with DCM. The combined organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The crude product was eluted over a silica gel with DCM/MeOH=1001 to 101 to give 12 g of 3-(tert-butyldiphenylsilyloxy)azetidine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266895B2
Source datasetuspto-grants-2016_02
ORD IDord-0652ca58e7f94ef0a03f0f98ec0ba0d0
Source noteuspto-grants-2016_02