HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80305Generated: October 30, 2026
Bromobenzene → [Diphenyl(4-pyridyl)]methanol
https://huagongshe.com/reaction/80305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Benzoylpyridine | HCID 26731 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Product | [Diphenyl(4-pyridyl)]methanol | HCID 67428383 | 97% |
Reaction Steps
A Grignard reagent was prepared from magnesium (0.21 g, 8.64 mmol) (Wako Pure Chemical Industries, Ltd.) and bromobenzene (1.35 g, 8.60 mmol) (Wako Pure Chemical Industries, Ltd.). 4-Benzoylpyridine (0.52 g, 28.4 mmol) (Wako Pure Chemical Industries, Ltd.) was dissolved in tetrahydrofuran (10 mL) (Wako Pure Chemical Industries, Ltd.), and the Grignard reagent was added dropwise, followed by stirring at room temperature for 5 hours. A saturated aqueous solution of ammonium chloride (Wako Pure Chemical Industries, Ltd.) was added to the reaction solution, and mixture was extracted with ethyl acetate (Wako Pure Chemical Industries, Ltd.). The organic layer was dried with anhydrous sodium sulfate (Wako Pure Chemical Industries, Ltd.), and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (chloroform (Wako Pure Chemical Industries, Ltd.) as an eluent), to thereby obtain the title compound (0.72 g, 97% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846012B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5f4e81eb6c9d44cca72f66321c991c50 |
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| Source note | uspto-grants-2014_09 |
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