HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256757Erstellt: 24. Oktober 2026
Dimethylamine → Diethyl ((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)methyl)phosphonate
https://huagongshe.com/de/reaction/256757
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylamine | HCID 674 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Triethyl phosphite | HCID 31215 | — |
| Edukt | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Edukt | 3-Hydro-2,2,5,6-tetramethylpyrazine | HCID 10261158 | — |
| Produkt | Diethyl ((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)methyl)phosphonate | HCID 70421 | — |
Reaktionsschritte
3.2 g of HTMP (hydroxymethylpiperidine), 52.3 g of paraformaldehyde and 206.3 g of 2,6-di-tert-butylphenol are rendered inert and are initially introduced at 60° C. under reduced pressure into a double-jacketed flask with an outlet at the bottom, a baffle, an impeller stirrer and a sublevel air lock for gas introduction. 52 g of dimethylamine gas are introduced at this temperature and the mixture is stirred at 85° C. for 1 hour. Addition of 332 g of triethyl phosphite is then carried out, after which the reaction mixture is kept at 115° C. for 4 hours. Working-up: distillation of triethyl phosphite and dimethylamine under reduced pressure and crystallization of the residue from ligroin yield 320 g of product (90%), melting point 114° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05258540 |
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| Quelldatensatz | uspto-grants-1993_11 |
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| ORD ID | ord-6e451c96394449579e8b8010653c5b12 |
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| Quellennotiz | uspto-grants-1993_11 |
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