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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271480Generated: November 1, 2026

Chlorotrimethylsilane → 3-(3-Chlorophenyl)-2-(difluoromethoxy)-5-(pyridin-2-ylmethyl)pyridine

https://huagongshe.com/reaction/2271480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1,2-DibromoethaneHCID 7839—
Reactant5-(Bromomethyl)-3-(3-chlorophenyl)-2-(difluoromethoxy)pyridineHCID 90415856—
ReactantHCID 178506410HCID 178506410—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Chlorophenyl)-2-(difluoromethoxy)-5-(pyridin-2-ylmethyl)pyridineHCID 90417189—

Reaction Conditions

Temperature70 °C

Reaction Steps

((5-(3-Chlorophenyl)-6-(difluoromethoxy)pyridin-3-yl)methyl)zinc(II) bromide. To a suspension of zinc (42.77 mg, 0.65 mmol) in THF (1 mL) was added 1,2-dibromoethane (2.48 μL, 0.03 mmol). The resulting mixture was heated at 70° C. for 10 minutes before being cooled to room temperature. Once cooled, trimethylsilylchloride (2.92 μL, 0.02 mmol) was added and the solution was stirred at room temperature for an additional 30 min. To the activated zinc solution was added 5-(bromomethyl)-3-(3-chlorophenyl)-2-(difluoromethoxy)pyridine (Intermediate 12, 200 mg, 0.57 mmol) and the resulting mixture was heated at 70° C. for 8 h. The reaction mixture was cooled to room temperature and decanted from the solids to afford a −0.5 M solution of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120770B2
Source datasetuspto-grants-2015_09
ORD IDord-4d3f8e1260264b8c9fde89fbfbd648fa
Source noteuspto-grants-2015_09