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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098173Generated: October 31, 2026

tert-Butyldimethylsilyl chloride → 3-((tert-Butyldimethylsilanyl)oxy)azetidine

https://huagongshe.com/reaction/1098173

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Hydroxyazetidine hydrochlorideHCID 2759290—
SolventDichloromethaneHCID 6344—
Product3-((tert-Butyldimethylsilanyl)oxy)azetidineHCID 5743865674%

Reaction Steps

A solution of tert-butylchlorodimethylsilane (12.01 g, 79.69 mmol) in DCM (20 mL) was added dropwise to a stirred solution of azetidin-3-ol hydrochloride (CAS no. 18621-18-6) (8.73 g, 79.69 mmol) and anhydrous N-ethyl-N-isopropylpropan-2-amine (34.1 mL, 199.22 mmol) in DCM (20 mL) cooled to 10° C., over a period of 2 minutes under nitrogen. The resulting solution was stirred at ambient temperature for 20 hours. The reaction mixture was concentrated, diluted with EtOAc (75 mL), and washed sequentially with saturated NaHCO3 (25 mL), water (20 mL), and saturated brine (20 mL). The organic layer was dried (MgSO4), filtered and evaporated to afford the product (11.1 g, 74%). 1H NMR (400 MHz, CDCl3) δ 0.04 (6H, s), 0.87 (9H, m), 2.80 (1H, s), 3.57-3.61 (2H, m), 3.67-3.71 (2H, m), 4.57-4.64 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143263B2
Source datasetuspto-grants-2012_03
ORD IDord-c1a2b3759e274760aefc60c382349073
Source noteuspto-grants-2012_03