HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588045Generated: October 30, 2026
Formaldehyde → Tetraethyl vinylidene phosphonate
https://huagongshe.com/reaction/1588045
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Tetraethyl methylenediphosphonate | HCID 15455 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tetraethyl vinylidene phosphonate | HCID 11022954 | — |
Reaction Steps
Paraformaldehyde (104.2 g) and diethylamine (50.8 g) are combined in methanol (2 1), warmed until clear, then treated with methylene bisphosphonic acid, tetraethyl ester (190.09 g) and refluxed for 18 hrs. The sample is then concentrated, methanol added, the methanol removed by heat and reduced pressure, toluene is added and removed by heat and reduced pressure. The residue is dissolved in toluene (1 1), treated with p-TSA (0.5 g) and refluxed through a Dean Stark trap for 18 hrs. The sample is concentrated under reduced pressure with heat, dissolved in methylene chloride washed twice with water, dried with magnesium sulfate, and concentrated under reduced pressure with heat. The sample is purified by distillation at reduced pressure to give the title compound, bp=140° (0.6 torr); MS (m/e) 300, 285, 273, 255, 245, 227, 217, 199, 192, 181, 163, 153 and 135; IR (neat) 2984, 2934, 2909, 1651, 1580, 1479, 1444, 1392, 1254, 1166, 1098, 1042, 1025, 974, 855, 813 and 800 cm-1 ; NMR (CDCl3) 7.1, 6.7, 4.1 and 1.3 δ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05220021 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-807e5c9d2609410883e51560287d330b |
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| Source note | uspto-grants-1993_06 |
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