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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorophenolHCID 4684—
Reactant4-FluorophenolHCID 9732—
ReactantPhosphorus trichlorideHCID 24387—
ReactantDiphenyl phosphiteHCID 62550—
ReactantPhenol, 4-fluoro-, 1,1',1''-phosphiteHCID 620022—
ReactantPhosphorusHCID 5462309—
ReactantPhosphorous acid, tris(4-chlorophenyl) esterHCID 5743262—
SolventTriethylamineHCID 8471—
ProductPhenol, 4-fluoro-, 1,1',1''-phosphiteHCID 620022—
ProductPhosphorous acid, tris(4-chlorophenyl) esterHCID 5743262—
ProductDi(4-chlorophenyl) phosphiteHCID 18515600—
ProductDi(4-fluorophenyl)phosphiteHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05543396
Source datasetuspto-grants-1996_08
ORD IDord-bbc132fab8804b82ad312ef9b2cedca0
Source noteuspto-grants-1996_08