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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656023Generated: November 2, 2026

Triphenylphosphine → HCID 19789980, compound

https://huagongshe.com/reaction/1656023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Chlorobenzyl alcoholHCID 13397—
ReactantHCID 19789982HCID 19789982—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19789980HCID 1978998062%

Reaction Steps

A mixture of 0.88 g of 2-chloro-4-(3-fluorophenoxy)phenol, 0.54 g of p-chlorobenzyl alcohol, 1.01 g of triphenylphosphine, 0.65 g of diethylazadicarboxylate and 90 ml of tetrahydrofuran was stirred at room temperature. After 48 hours, the reaction mixture was concentrated, and 50 ml of diethyl ether was added thereto. The precipitates were removed by filtration, and the filtrate was concentrated. The residue was subjected to silica gel chromatography to give 0.83 g of 4-chloro-1-[2-chloro-4-(3-fluorophenoxy)phenoxy]methylbenzene. Yield, 62%. m.p., 47.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252610
Source datasetuspto-grants-1993_10
ORD IDord-cab897fe987d463181f4d0671b04d049
Source noteuspto-grants-1993_10