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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-4-phenylmethoxybenzene | HCID 138835 | — |
| Reactant | 1-Bromo-4-pentylbenzene | HCID 2735599 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-n-Pentyl-4'-benzyloxybiphenyl | HCID 22925898 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534547B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-8d20c04849414269beea7df1f151b610 |
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| Source note | uspto-grants-2009_05 |
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