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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516145Generated: October 29, 2026

Triethylamine → Tert-butyl 3-(methanesulfonyloxy)azetidine-1-carboxylate

https://huagongshe.com/reaction/516145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductTert-butyl 3-(methanesulfonyloxy)azetidine-1-carboxylateHCID 10753243—

Reaction Steps

N-Boc-3-hydroxyazetidine (1.73 g) was dissolved in chloroform (20 ml). Triethylamine (2.09 ml) and methanesulfonyl chloride (856 μl) were added thereto at 0° C. After stirring at room temperature for 0.5 hours, ethyl acetate and water were added thereto to separate the organic layer. After being washed with a saturated aqueous sodium bicarbonate solution, a saturated aqueous ammonium chloride solution, and water, the organic layer was dried over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure to obtain the title compound as a colorless, oily compound (2.32 g). Physical properties: m/z [M+H]+ 252.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108973B2
Source datasetuspto-grants-2015_08
ORD IDord-e666a340e54c48fd8b72f935cf5971c0
Source noteuspto-grants-2015_08