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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950302Generated: October 29, 2026

Diethyl Ether → 2-(3'-Benzyloxy-5-methoxybiphenyl-2-yl)-6-methoxynaphthalene

https://huagongshe.com/reaction/1950302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantIsoamyl NitriteHCID 8053—
ReactantTetrafluoroboric acidHCID 28118—
Reactant5-Methoxy-2-(6-methoxynaphthalen-2-yl)phenylamineHCID 23087511—
SolventTetrahydrofuranHCID 8028—
Product2-(3'-Benzyloxy-5-methoxybiphenyl-2-yl)-6-methoxynaphthaleneHCID 23087183—

Reaction Conditions

Temperature-40 °C

Reaction Steps

The title compound was synthesized by referring to Tetrahedron Lett., 1996, 37, 3857. To a solution of 5-methoxy-2-(6-methoxynaphthalen-2-yl)phenyl amine (340 mg) in tetrahydrofuran (8 ml) was added tetrafluoroboric acid (42% aqueous solution) (0.22 ml) under a nitrogen atmosphere, the solution was cooled at −40° C., isoamyl nitrite (2.4 ml) was then added dropwise thereto followed by stirring for 2 hours at −40° C. Diethyl ether (20 ml) was added thereto and the solid that was precipitated was filtered. A suspension of the resulting 5-methoxy-2-(6-methoxynaphthalen-2-yl)benzenediazonium tetrafluoroborate (320 mg), 3-benzyloxyphenylboronic acid (235 mg) and palladium(II) acetate (10 mg) in 1,4-dioxane (4 ml) was stirred overnight at room temperature under a nitrogen atmosphere. Water was added thereto followed by stirring, the solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (181 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399520B2
Source datasetuspto-grants-2013_03
ORD IDord-a8042ce783a942ab9c9098e7b1a7e581
Source noteuspto-grants-2013_03