HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925200Generated: October 29, 2026
3-Bromopyridine → HCID 86725312, compound
https://huagongshe.com/reaction/925200
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | HCID 86725304 | HCID 86725304 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86725312 | HCID 86725312 | — |
Reaction Steps
To a stirred solution of 3-bromopyridine (0.11 ml, 1.13 mmol) in THF (5 ml) under Ar at −78° C., n-BuLi (2.5 M in hexane, 0.45 ml, 1.13 mmol) was added. The mixture was stirred at −78° C. for 20 minutes, followed by dropwise addition of Intermediate 1 (0.15 g, 0.38 mmol) in THF (5 ml). The mixture was stirred for 2 h at −78° C., allowed to warm to room temperature, and quenched by slow addition of aqueous saturated NH4Cl (50 ml). The mixture was extracted with EtOAc (3×). The combined EtOAc extracts were washed with brine, dried (Na2SO4), and solvent evaporated in vacuo to give the sub-title compound as tan oil that was used without further purification. MS: ESI (positive): 479 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284277B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-6216cd49c0ca48af9d361e96ea0c0934 |
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| Source note | uspto-grants-2016_03 |
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