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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470109Generated: October 26, 2026

Triethylamine → Diethyl 2-(chlorosulfonylamino)ethylphosphonate

https://huagongshe.com/reaction/1470109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
ReactantDiethyl (2-aminoethyl)phosphonateHCID 2733596—
SolventDichloromethaneHCID 6344—
ProductDiethyl 2-(chlorosulfonylamino)ethylphosphonateHCID 86672335—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 100-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of sulfuryl dichloride (1.1 g, 8.15 mmol, 1.47 equiv) in dichloromethane (10 mL). This was followed by the addition of a solution of diethyl 2-aminoethylphosphonate (intermediate 1.9) (1.0 g, 5.52 mmol, 1.00 equiv) and triethylamine (800 mg, 7.92 mmol, 1.43 equiv) in dichloromethane (20 mL) dropwise with stirring at 0° C. The resulting solution was stirred for 2 h at 0° C. The reaction was then quenched by the addition of ice water. The organic layer was washed with saturated sodium chloride (20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 0.5 g (crude) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006281B2
Source datasetuspto-grants-2015_04
ORD IDord-6d1db532f7ae4ba5938376e9c1186c42
Source noteuspto-grants-2015_04