HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2199366Erstellt: 24. Oktober 2026
Tributylamine → 1-Butanamine, N,N-dibutyl-, hydrochloride (1:1)
https://huagongshe.com/de/reaction/2199366
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tributylamine | HCID 7622 | — |
| Edukt | Butylamine | HCID 8007 | — |
| Edukt | Thiophosphoryl chloride | HCID 19883 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-Butanamine, N,N-dibutyl-, hydrochloride (1:1) | HCID 80570 | — |
Reaktionsschritte
To this end, thiophosphoryl chloride and a primary alkylamine, for example n-butylamine, are reacted in molar ratios of preferably 0.9 to 1.1 mol of amine per mole of thiophosphoryl chloride in an inert solvent, for example ethyl acetate. The auxiliary base used is a trialkylamine, for example tri-n-butylamine, which is reacted to give the tri-n-butylamine hydrochloride. In a second reaction step, the N-alkylthiophosphoryl dichloride which has been formed in the first reaction is reacted with ammonia at temperatures of between preferably −20° C. and 50° C. to give the desired product N-alkylthiophosphoric triamide. In parallel with, and independently of, the second reaction step, ammonia acts as base 2 and accepts the hydrogen chloride from the trialkylamine hydrochloride with formation of ammonium chloride.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09359269B2 |
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| Quelldatensatz | uspto-grants-2016_06 |
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| ORD ID | ord-8c1ccd5fe3ab4d7b80831e24ad302a51 |
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| Quellennotiz | uspto-grants-2016_06 |
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