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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479374Generated: November 1, 2026

Triethylamine → Diethyl 2-(chlorosulfonylamino)ethylphosphonate

https://huagongshe.com/reaction/1479374

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 numberUS09408840B2
Source datasetuspto-grants-2016_08
ORD IDord-d60148665bbc415a9121d782c3cf3426
Source noteuspto-grants-2016_08