HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077566Generated: November 2, 2026
4-Chlorophenol → Phenol, 4-fluoro-, 1,1',1''-phosphite
https://huagongshe.com/reaction/1077566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorophenol | HCID 4684 | — |
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Diphenyl phosphite | HCID 62550 | — |
| Reactant | Phenol, 4-fluoro-, 1,1',1''-phosphite | HCID 620022 | — |
| Reactant | Phosphorus | HCID 5462309 | — |
| Reactant | Phosphorous acid, tris(4-chlorophenyl) ester | HCID 5743262 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Phenol, 4-fluoro-, 1,1',1''-phosphite | HCID 620022 | — |
| Product | Phosphorous acid, tris(4-chlorophenyl) ester | HCID 5743262 | — |
| Product | Di(4-chlorophenyl) phosphite | HCID 18515600 | — |
| Product | Di(4-fluorophenyl)phosphite | HCID 19431395 | — |
Reaction Steps
Di(4-chlorophenyl) phosphite and di(4-fluorophenyl) phosphite were prepared from tris(4-chlorophenyl) phosphite and tris(4-fluorophenyl) phosphite, respectively using a previously described procedure (Walsh, E. N., Conversion of Tertiary Phosphites to Secondary Phosphonates. Diphenyl Phosphonate, J. Am. Chem. Soc. 1959, 81, 3023-6). Tris(4-chlorophenyl) phosphite was prepared from 4-chlorophenol and phosphorous trichloride with three equivalents of triethyl amine as a base using a modification of a previous procedure (McCombie, H., Saunders, B. C., Stacey, G. J., Esters Containing Phosphorus. Part I, J. Chem. Soc. 1945, 381). Similarly, tris(4-fluorophenyl) phosphite was prepared from 4-fluorophenol and phosphorous trichloride using one equivalent of triethyl amine as a base.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05543396 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-bbc132fab8804b82ad312ef9b2cedca0 |
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| Source note | uspto-grants-1996_08 |
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