Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Triphenyl phosphite | HCID 7540 | — |
| Catalyst | Methyl iodide | HCID 6328 | — |
| Product | Diphenyl methylphosphonate | HCID 82027 | 92% |
Reaction Steps
A reactor fitted with an efficient condenser, thermometer, mechanical stirrer and side-arm addition funnel was charged with 1552 g (5.0 mol) of triphenyl phosphite. The reactant was placed under a nitrogen blanket and heated to reflux. A solution of 5.0 g of methyl iodide in 160 g (5.1 mol) of methanol was then slowly added over a two hour period. Throughout the addition, the temperature of the reactor contents was maintained within the 200°-250° C. range. One further hour at 215° C. proved sufficient for the reaction to reach completion. Subsequently, as aspirator vacuum distillation removed 468 g (5.0 mol) of phenol containing a small amount of anisole. Thereafter, a high vacuum distillation recovered 1150 g (4.6 mol, 92% yield) of diphenyl methylphosphonate. Glc analysis using a 6 foot column packed with 10% OV-101 on chromosorb W, was employed to monitor the progress of both the reaction and distillation. The s:p signal for the product appeared at -24.0 ppm. Proton nmr signals were seen at τ8.36 (3H, doublet, J=18 HZ, CH3P) and τ2.9-2.5 (10H, multiplet, phenyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04276234 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-ada3a354c1484421b531995e9e87b910 |
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| Source note | uspto-grants-1981_06 |
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