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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346440Generated: October 30, 2026

Triethylamine → N-(4-Chlorobutyl)-N-methylphosphoramidic dichloride

https://huagongshe.com/reaction/346440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Chloro-N-methylbutan-1-amine--hydrogen chloride (1/1)HCID 55302560—
SolventDichloromethaneHCID 6344—
ProductN-(4-Chlorobutyl)-N-methylphosphoramidic dichlorideHCID 1164438185%

Reaction Conditions

Temperature-40 °C

Reaction Steps

N-methyl-N-(4-chlorobutyl)amine hydrochloride (2.0 g, 12.73 mmol) was dissolved in 20 mL of anhydrous CH2Cl2 and cooled to −40° C. Phosphorous oxycloride (1.2 mL, 12.73 mmol) was added neat followed by the drop wise addition of triethyl amine (3.6 mL, 25.46 mmol) in 5 mL of CH2Cl2. Warmed reaction to 0° C. and slowly to room temperature. Allowed reaction to stir at room temperature for 6 hours. The reaction mixture was poured over ice, added saturated ammonium chloride and separated layers. Extracted water layer 3× with CH2Cl2, combined organic layers, dried over anhydrous sodium sulfate and concentrated under reduce pressure. Purified by silica gel flash chromatography (3:1 Hex/EtOAc) to yield a clear oil (2.57 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173020B2
Source datasetuspto-grants-2007_02
ORD IDord-e7039ddf8f3b4248b144eddecba0c8d8
Source noteuspto-grants-2007_02