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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359964Generated: October 31, 2026

4-Methylpyridine → HCID 18446302, compound

https://huagongshe.com/reaction/1359964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpyridineHCID 7963—
ReactantAmmonium ChlorideHCID 25517—
ReactantBromocyclopropaneHCID 78037—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18446302HCID 1844630266%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of 19.5 ml (200 mmol) of 4-picoline in tetrahydrofuran (120 ml) was cooled to −78° C. Lithium diisopropylamide (2 M heptane, tetrahydrofuran, ethylbenzene solution) (200 ml) was added dropwise to the cooled solution over a period of 20 min. The mixture was then stirred at -40° C. for 20 min and was cooled to −78° C. Cyclopropylbromide (16.0 ml, 200 mmol) was added dropwise to the reaction solution over a period of 25 min, and the mixture was stirred at −78° C. for one hr. The reaction solution was then added to 300 ml of a saturated aqueous ammonium chloride solution, and the mixture was satisfactorily washed with 100 ml of water. The solution was extracted twice with 200 ml of ethyl acetate, and the extract was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated, and the residue was distilled under the reduced pressure (8 mmHg, 86 to 87° C.). The distillation residue was purified by column chromatography on silica gel (hexane:ethyl acetate=70:30) to give 17.6 g (yield 66%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879808B2
Source datasetuspto-grants-2011_02
ORD IDord-b064d8f8eddb4023b3b6fe00f9ab53f9
Source noteuspto-grants-2011_02