HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374233Generated: October 29, 2026
Hydrogen Bromide → Phosphonic acid, p-phenylenedi-
https://huagongshe.com/reaction/374233
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tetraethyl 1,4-phenylenebisphosphonate | HCID 88843 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Phosphonic acid, p-phenylenedi- | HCID 2773663 | 88.1% |
Reaction Steps
93 ml of HBr at 33% by weight in acetic acid are added to 6.68 g of 1.4-benzene-diphosphonic acid tetra-ethyl ester and the mixture is heated to 80° C. for 4 hours. After cooling to ambient temperature 200 ml of diethyl-ether are added and the mixture, after brief agitation, is cooled to -78° C. in a bath of ethanol and dry ice. The oily precipitate obtained is recovered by decantation and subjected twice more to the dispersion process with ether and low-temperature precipitation. The oily residue obtained is vacuum dried (1 mm Hg) at 50° C. for 8 hours, obtaining 4.0 g of 1,4-benzene-diphosphonic acid in the form of a white solid. Yield in moles 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166380 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-5c6ab400d847403098c04a1f9d69b829 |
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| Source note | uspto-grants-1992_11 |
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