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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410490Generated: October 25, 2026

Diisopropylethylamine → Tert-butyl 3-{[(dimethylphosphoryl)oxy]methyl}azetidine-1-carboxylate

https://huagongshe.com/reaction/410490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantDimethylphosphinic chlorideHCID 517954—
Reactanttert-Butyl 3-(hydroxymethyl)azetidine-1-carboxylateHCID 10583745—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-{[(dimethylphosphoryl)oxy]methyl}azetidine-1-carboxylateHCID 6743195869.7%

Reaction Steps

Diisopropyl ethyl amine (124.28 g, 0.961 mol) was added dropwise to stirred solution of compound tert-butyl 3-(hydroxymethyl)azetidine-1-carboxylate (150 g, 0.80 mol) in dichloromethane (500 mL) at 0° C. Dimethyl phosphinyl chloride (90 g, 0.80 mol) in dichloromethane (300 mL) was added to above reaction mixture over a period of 90 min at same temperature. Then, the reaction mixture was warmed to room temperature and continued stirring for 2 h. After completion of the reaction, the mixture was diluted with water (300 mL). The layers were separated. The organic layer was washed with brine (300 ml), dried over sodium sulfate and concentrated. The resultant concentrated product was purified via column chromatography on silica gel using chloroform/methanol (95/5) to afford tert-butyl 3-{[(dimethylphosphoryl)oxy]methyl}azetidine-1-carboxylate (146.8 g, 68.3%) as brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-2769a50fc53f43c2965f1d6307bf0cdb
Source noteuspto-grants-2014_06