Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diketene | HCID 12661 | — |
| Reactant | HCID 131712988 | HCID 131712988 | — |
| Reactant | HCID 178443311 | HCID 178443311 | — |
| Product | HCID 13718265 | HCID 13718265 | — |
Reaction Steps
A mixture of 13.2 parts of dodecyl methylphosphite, 4.2 parts of diketene and 0.6 parts of bis-(t-butylcyclohexyl)-perdicarbonate was added dropwise over 30 minutes to 39.6 parts of dodecylmethylphosphite which was vigorously stirred at 85° C. in a nitrogen atmosphere. On completion of the addition the reaction mixture was heated for a further 30 minutes at 85° C., then the excess of dodecylmethylphosphite was removed on a wiped wall still at a wall temperature of 80° C. and pressure 0.013 mb. The residue was distilled on a wiped wall still at a wall temperature of 150° C. and pressure 0.013 mb, and gave dodecyl methyl 2-oxo-4-oxetanylmethylphosphonate as a colourless oil which had the following analysis by weight:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04384966 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-4bfb9e8ee5ac41ad868210490865445c |
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| Source note | uspto-grants-1983_05 |
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