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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Chloro-N-methylbutan-1-amine--hydrogen chloride (1/1) | HCID 55302560 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Chlorobutyl)-N-methylphosphoramidic dichloride | HCID 11644381 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173020B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-e7039ddf8f3b4248b144eddecba0c8d8 |
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| Source note | uspto-grants-2007_02 |
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