HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466647Generated: October 29, 2026
1-Bromo-4-iodobenzene → 4'-Bromo-2-methyl-1,1'-biphenyl
https://huagongshe.com/reaction/466647
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-4-iodobenzene | HCID 11522 | — |
| Reactant | HCID 178424303 | HCID 178424303 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Bromo-2-methyl-1,1'-biphenyl | HCID 15205876 | 82% |
Reaction Steps
A stirred solution of 21.0 mL of (2-methylphenyl)magnesium bromide (42.0 mmol, 2.0M in diethyl ether) was evaporated in situ at room temperature. The syrupy residue was redissolved in 50 mL of THF and cooled to -20° C. under argon. To this solution was added a solution of 6.84 g (50.0 mmol) of thricefused zinc chloride. The resulting thick white slurry was warmed to room temperature and stirred for 1 hour. After cooling to -78° C., a solution of 11.32 g (40.0 mmol) of 1-bromo-4-iodobenzene and 500 mg (0.4 mmol) of tetrakis(triphenylphosphine)palladium in 50 mL of THF was added over the course of thirty minutes. After an additional 20 minutes, the cooling bath was removed, the reaction stirred at room temperature for 2 hours and then quenched with 100 mL of 1M hydrochloric acid. The mixture was extracted twice with hexanes, the extracts combined, washed once with saturated sodium bicarbonate solution and once with 10% sodium thiosulfate. The organic extract was dried (MgSO4) and evaporated. The crude product (11.3 g) was purified by distillation (bp 93°-95° C. at 0.5 Torr) to give 8.06 g (82%) of title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157027 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-d617cd918b464deabe1c3fe33495ba34 |
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| Source note | uspto-grants-1992_10 |
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