HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48044Generated: October 28, 2026
Hydrochloric Acid → 3-(Pyridin-2-yl)benzaldehyde
https://huagongshe.com/reaction/48044
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Pyridin-2-yl)benzaldehyde | HCID 3710039 | 38.2% |
Reaction Steps
Ex-587A) To a THF solution (8 mL) of 2-bromopyridine (1.30 g, 8.23 mmol) at −78° C. was added 1.6 M n-BuLi in hexanes (5.3 mL, 8.48 mmol). The resulting dark red solution was stirred at −78° C. for 10 min, and a solution of 0.5 M ZnCI2 in THF (18 mL, 9.0 mmol) was added giving a light brown slurry. After warming to room temperature, 3-bromobenzaldehyde (0.816 mL, 7.0 mmol) and Pd(PPh3)4 (0.242 g, 0.21 mmol) were added, and the mixture was stirred for 18 h at room temperature under argon. The reaction mixture was poured into 1 N HCl (30 mL) and washed with diethyl ether. The aqueous layer was neutralized with NaHCO3 and extracted with diethyl ether. The solvent was removed in vacuo to give the crude product as an oil. Purification by flash chromatography on silica gel eluting with 20% ethyl acetate in hexane gave 0.49 g (38%) of the desired 3-(2-pyridinyl)benzaldehyde product as a colorless oil. GCMS: m/z=183 [M+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06699898B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-51551e47c08d40f780073ed798d6e6a3 |
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| Source note | uspto-grants-2004_03 |
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