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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222315Generated: October 31, 2026

Ammonium Chloride → (2,5-Dichloropyridin-3-yl)(2-fluoro-3-methoxy-6-vinylphenyl)methanol

https://huagongshe.com/reaction/222315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Bromo-2,5-dichloropyridineHCID 12901596—
Reactant2-Fluoro-3-methoxy-6-vinylbenzaldehydeHCID 57722773—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventDiisopropyl EtherHCID 7914—
Product(2,5-Dichloropyridin-3-yl)(2-fluoro-3-methoxy-6-vinylphenyl)methanolHCID 86609785—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207186B2
Source datasetuspto-grants-2012_06
ORD IDord-b2fb74cdb25045bfaae5b9c74f8539f0
Source noteuspto-grants-2012_06