Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178527008 | HCID 178527008 | — |
Reaction Steps
3,9-Dioxo-3,9-diphospha-2,4,8,10-tetraoxa-spiro[5.5]undecane was prepared as follows. Under stirring and a nitrogen atmosphere a suspension of 68 g of pentaerythitol, 152 g of diethylphosphite, and 73 g of water-free tetraline was heated to 135° C. At 135° C., 55% of the theoretical amount of ethanol were removed from the reaction mixture over a period of 3 h. The pressure was diminished slowly to 10 kPa and more ethanol was removed at 135° C. After cooling to 80° C., 60 g of methanol were added after which the methanol layer with the product was separated from the tetraline layer. After evaporation at a 95° C. and a pressure of 0.2 kPa, 100 g of a viscous product were obtained, which crystallized on standing at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06284869B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-c4d02eadc1c946ec8379acdc40aee9b1 |
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| Source note | uspto-grants-2001_09 |
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