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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601681Generated: October 30, 2026

Triethylamine → 3-Methoxy-cyclobutylmethylazide

https://huagongshe.com/reaction/601681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
Reactant(3-Methoxycyclobutyl)methanolHCID 23158380—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-Methoxy-cyclobutylmethylazideHCID 2315833572.9%

Reaction Steps

530 μl of triethylamine followed by 220 μl of methanesulfonylchloride were added under iced temperature to 220 mg of 1) 3-methoxy-cyclobutylmethanol obtained in the above 1). The mixture was heated to room temperature and stirred for 30 min. The reaction solution was diluted with ethyl acetate, washed with water, saturated sodium bicarbonate water and saturated saline solution, and dried with anhydrous sodium sulfate. The residues obtained by evaportating the solvents under reduced pressure were dissolved in 4 ml of dimethylformamide. Then, 245 mg of sodium azide was added, and the mixture was stirred at 80° C. for 1.5 hours. The reaction solution was diluted with ethyl acetate, washed with water and saturated saline solution and dried with anhydrous sodium sulfate. The residues obtained by distilling out the solvents under reduced pressure were separated and purified by silicagel column chromatography (ethyl acetate:hexane=10:90) to obtain 195 mg of the above compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-bf530e4ce0074f84884d1ad667b1d969
Source noteuspto-grants-2011_03