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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493038Generated: October 27, 2026

1-Bromo-4-phenylmethoxybenzene → 4-n-Pentyl-4'-benzyloxybiphenyl

https://huagongshe.com/reaction/493038

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-phenylmethoxybenzeneHCID 138835—
Reactant1-Bromo-4-pentylbenzeneHCID 2735599—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product4-n-Pentyl-4'-benzyloxybiphenylHCID 2292589862%

Reaction Steps

Magnesium (1.06 g: 88.3 mmol) and 4-n-pentylbromobenzene (10.0 g: 44.01 mmol) were dissolved in 50 ml of dried tetrahydrofuran, and a Grignard reagent was prepared from the mixture. To the Grignard reagent was added 11.6 g (44.1 mmol) of 4-(benzyloxy)bromobenzene synthesized in the step (i). The reaction system was purged with argon. To the reaction system was added 600 mg of dichloro(1,4-diphenylphosphinobutane)palladium (II) [Pd(dppb)Cl2], and the reaction was conducted for 24 hours. The reaction mixture was poured into an iced water, and the resultant mixture was acidified by adding hydrochloric acid. The resultant solid was collected by filtration, washed with water, dried, and recrystallized from a mixed solvent of hexane/toluene to give 9.0 g (27.3 mmol) of 4-n-pentyl-4′-benzyloxybiphenyl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534547B2
Source datasetuspto-grants-2009_05
ORD IDord-8d20c04849414269beea7df1f151b610
Source noteuspto-grants-2009_05