HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987142Generated: October 30, 2026
Ammonium Chloride → (2,5-Dichloropyridin-3-yl)(2-fluoro-3-methoxy-6-vinylphenyl)methanol
https://huagongshe.com/reaction/1987142
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Bromo-2,5-dichloropyridine | HCID 12901596 | — |
| Reactant | 2-Fluoro-3-methoxy-6-vinylbenzaldehyde | HCID 57722773 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | (2,5-Dichloropyridin-3-yl)(2-fluoro-3-methoxy-6-vinylphenyl)methanol | HCID 86609785 | — |
Reaction Steps
To a stirred solution of nBuLi (1.6 M in hexane, 29.0 mL, 46.4 mmol) in diisopropyl ether (80 mL) was added 3-bromo-2,5-dichloropyridine (10.5 g, 46.4 mmol) in diisopropylether (60 mL) slowly at −78° C. The resulting suspension was treated with 2-fluoro-3-methoxy-6-vinylbenzaldehyde (7.6 g, 42.2 mmol) in diisopropylether (60 mL) and benzene (3 mL), and allowed to stir at −78° C. for 30 min followed by warming to room temperature as the bath did. The mixture was treated with saturated NH4Cl solution and extracted with EtOAc (×3). The combined organics were washed with brine, dried (Na2SO4), concentrated, and purified by flash chromatography to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550478B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-006c1b9c4aad460b908701196ca4ad03 |
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| Source note | uspto-grants-2009_06 |
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