HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270236Generated: October 30, 2026
Methyl iodide → Diphenyl methylphosphonate
https://huagongshe.com/reaction/270236
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Triphenyl phosphite | HCID 7540 | — |
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Product | Diphenyl methylphosphonate | HCID 82027 | — |
Reaction Steps
To a three-necked flask equipped with thermometer, magnetic stirrer, distillation head and nitrogen inlet 163 g (0.52 mol) of triphenyl phosphite and 1.0 mL of methyl iodide were charged. Then, 32.7 g (0.26 mol) of trimethyl phosphite was added drop-wise at 100–110° C. over the course of one hour. The reaction temperature was then raised to 210° C. and an exothermic reaction was observed. The reaction temperature was maintained at 230° C. for two hours, and the reaction mixture was analyzed before it underwent transesterification. Diphenyl methylphosphonate was obtained as a liquid. The 31P NMR (CDCl3) indicated 95% diphenyl methylphosphonate. The impurities included triphenyl phosphate (0.8%, δ=−16.4 ppm), trimethyl phosphate (0.6%, δ=−10.3 ppm), and unknown compounds (δ=19.8, 20.4. 28.4 ppm). The acid number of this crude diphenyl methylphosphonate was 5.4 mg KOH/g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449526B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-aff8533de1374141a8909be6d4980c4c |
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| Source note | uspto-grants-2008_11 |
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