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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937656Generated: October 30, 2026

Phenol → e-4-[4-(2-Benzyloxyethoxy)phenyl]-3,4-diphenyl-but-3-en-1-ol

https://huagongshe.com/reaction/1937656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantBenzene, ((2-bromoethoxy)methyl)-HCID 73833—
ReactantHCID 13298066HCID 13298066—
Producte-4-[4-(2-Benzyloxyethoxy)phenyl]-3,4-diphenyl-but-3-en-1-olHCID 22461338—

Reaction Steps

The alkylation of the starting phenol with benzyl-(2-bromoethyl)ether was carried out as described in Example 1 of the International Patent Application WO 96/07402 with the exception that now the starting compound was the other geometric isomer, E-4-(4-hydroxy-1,2-diphenyl-but-1-enyl)-phenol which was prepared by the method described in U.S. Pat. No. 4,996,225. The product was extracted to toluene. The toluene phases were combined, washed with water, dried and evaporated to dryness. The residue was recrystallized from a minor quantity of toluene and the precipitated product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395785B1
Source datasetuspto-grants-2002_05
ORD IDord-2d438b6e82494ca1a1389d48de792f0d
Source noteuspto-grants-2002_05