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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193661Generated: November 2, 2026

2-Bromopyridine → HCID 10703742, compound

https://huagongshe.com/reaction/1193661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantSodium hydrideHCID 24758—
ReactantBenzeneacetonitrile, 4-fluoro-HCID 68016—
SolventWaterHCID 962—
ProductHCID 10703742HCID 1070374228.6%

Reaction Steps

A sample of sodium hydride (60%, 1.60 g, 0.04 mole) was washed with dry hexanes. After removal of hexanes a 100 ml portion of dimethyl sulfoxide was added. To this mixture was added a solution of 4-fluorophenylacetonitrile (5.41 g, 0.04 mole). The mixture was stirred 3 hrs at room temperature under nitrogen. 2-Bromopyridine (6.32 g, 0.04 mole) was added to the mixture, the reaction mixture was then stirred overnight at 65° C. The reaction mixture was poured into 1200 ml of water and the aqueous phase was extracted several times with chloroform (the chloroform layer was filtered using Celite). The combined chloroform layer was extracted with water and 5% sodium hydroxide. The chloroform layer was dried over sodium sulfate, filtered, and solvent removed to give a red oil. The oil was subjected to flash chromatography on silica gel using 10% ethylacetate-90% hexanes and 20% ethylacetate-80% hexanes for elution. Fractions of similar purity was combined and solvent removed in vacuo. The oil obtained was dried in vacuo overnight at 80° C. to give 2.43 g (28.6%) of clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810713
Source datasetuspto-grants-1989_03
ORD IDord-593e30d33511448184404adbc43a8d0a
Source noteuspto-grants-1989_03