HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908540Generated: October 30, 2026
Benzophenone → Diphenyl(pyridin-3-yl)methanol
https://huagongshe.com/reaction/908540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diphenyl(pyridin-3-yl)methanol | HCID 298509 | 20% |
Reaction Steps
A solution of 3-bromopyridine (10 g, 0.063 mol) in dry THF (200 mL)/hexane (50 mL) was cooled to −90° C. To this cooled solution was added n-BuLi (2.2 M, 32 mL, 0.063 mol) slowly and allowed to stir for 30 min under N2 atmosphere. A solution of benzophenone (11.5 g, 0.063 mol) in dry THF (50 mL) was added to this at the same temperature over a period of 30 min. The reaction mixture was warmed slowly to RT and allowed to stir another 3 h at RT. The reaction mixture was cooled, quenched with water (200 mL) and extracted with ethyl acetate (2×100 mL). The organic layer was dried, concentrated under vacuum and the crude product was purified by column chromatography on silica gel (30% ethyl acetate in pet. ether) which gave the title compound (3.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017620B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-286d3f1566c7432b833b78d130bd39bb |
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| Source note | uspto-grants-2011_09 |
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