HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500322Generated: October 26, 2026
Boron trifluoride etherate → 4-Bromo-1-chloro-2-(4-methoxybenzyl)benzene
https://huagongshe.com/reaction/500322
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (5-Bromo-2-chloro-phenyl)-(4-ethoxy-phenyl)-methanone | HCID 22328608 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-1-chloro-2-(4-methoxybenzyl)benzene | HCID 22328594 | — |
Reaction Steps
A solution of 86.2 g (5-bromo-2-chloro-phenyl)-(4-methoxy-phenyl)-methanone and 101.5 mL triethylsilane in 75 mL dichloromethane and 150 mL acetonitrile is cooled to 10° C. 50.8 mL of boron trifluoride etherate are added so that the temperature does not exceed 20° C. The solution is stirred for 14 h at ambient temperature, before another 9 mL triethylsilane and 4.4 mL boron trifluoride etherate are added. The solution is stirred for a further 3 h at 45 to 50° C. and then cooled to ambient temperature. A solution of 28 g potassium hydroxide in 70 mL of water is added, and the resultant mixture is stirred for 2 h. Then the organic phase is separated, and the aqueous phase is extracted three times with diisopropylether. The combined organic phases are washed twice with 2 M potassium hydroxide solution and once with brine and then dried over sodium sulfate. After the solvent is removed, the residue is washed with ethanol and dried at 60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772191B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-12fd880a19aa4874a89a1eda5be596bd |
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| Source note | uspto-grants-2010_08 |
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