Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | O-Xylene | HCID 7237 | — |
| Edukt | Benzotrichloride | HCID 7367 | — |
| Edukt | Diethylphosphite | HCID 3780918 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Phenyl methane triphosphonic acid | HCID 56631278 | — |
Reaktionsschritte
There were mixed together 23.0 grams (1.0 mole) of sodium metal along with 90 cc. of xylene and 80 cc. of tetrahydrofurane and the mixture placed under a nitrogen atmosphere. There were then added over a 35 minute period 138.10 grams (1.0 mole) of diethyl phosphite using external cooling to control the reaction exotherm and maintain the temperature at 60° to 65° C. After addition was complete the mixture was heated to 100° C. and maintained there for about 1 hour until there was no more sodium. The mixture was cooled to 60° C. and there was started the addition of 64.5 grams (0.33 mole) of benzotrichloride (α,α,α-trichlorotoluene). The exothermic reaction was cooled to maintain the temperature at 60° to 65° C. during the 25 minute addition period. The mixture was heated at 70° to 75° C. for 7 hours and the sodium chloride filtered off. The product in the pot was then subjected to distillation, terminal conditions being a pot temperature of 205° C., distillate temperature 125° C. and pressure 4 mm. The solid residue in the pot was hexaethyl phenyl methane triphosphonate. This product was hydrolyzed and the hydrolysis product purified as in Example 1 to obtain phenyl methane triphosphonic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04440646 |
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| Quelldatensatz | uspto-grants-1984_04 |
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| ORD ID | ord-d5b3d9f94fa24099a44ac1f651a10d52 |
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| Quellennotiz | uspto-grants-1984_04 |
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