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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713558Generated: November 2, 2026

5-Chloro-2-phenylpyridine → 5-Ethyl-2-phenylpyridine

https://huagongshe.com/reaction/713558

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-phenylpyridineHCID 2762866—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Product5-Ethyl-2-phenylpyridineHCID 59785319%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Chloro-2-phenylpyridine (16 g, 84 mmol) and Ni(dppe)Cl2 (0.891 g, 1.687 mmol) were added to 300 mL of THF and the reaction mixture was degassed with nitrogen for 20 min. before being cooled to 0° C. Ethylmagnesium bromide (169 mL, 169 mmol) was added dropwise over a period of 60 min. and the reaction mixture stirred for and additional 3 h at before warming to room temperature overnight. The reaction mixture was recooled to 0° C. and quenched with 250 mL of water, extracted with EtOAc and the organic layer dried over sodium sulfate and filtered. The crude material was chromatographed on silica with 95/5 hexane/EtOAc to give 2.9 g (19%) of 5-ethyl-2-phenylpyridine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09184397B2
Source datasetuspto-grants-2015_11
ORD IDord-501eb203d6c542168dea71438a871f8d
Source noteuspto-grants-2015_11