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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446749Generated: October 29, 2026

Lithium Chloride → HCID 178501137, compound

https://huagongshe.com/reaction/446749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
Reactant3-Bromo-2-chloropyridineHCID 693324—
ReactantMagnesiumHCID 5462224—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 178501148HCID 178501148—
CatalystTetrahydrofuranHCID 8028—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178501137HCID 17850113746%

Reaction Steps

To a mixture of lithium chloride (0.55 g, 13 mmol) and magnesium turnings (0.63 g, 26 mmol) in dry tetrahydrofuran (34 ml) was added 1M diisobutyl aluminum hydride solution in tetrahydrofuran (0.10 ml, 0.10 mmol) at room temperature. After stirring for 5 minutes a solution of 3-bromo-2-chloro-pyridine (2.00 g, 10.4 mmol) in dry tetrahydrofuran (1 ml) was added at 0-5° C. Stirring for 1 h was followed by addition of a solution of zinc chloride (1.42 g, 10.4 mmol), which had previously been dried by melting in vacuo followed by cooling under argon, in dry tetrahydrofuran (10 ml). After stirring for 1 h the mixture was decanted into another flask by cannulation under argon. Addition of tetrakis(triphenylphosphine)palladium(0) (0.59 g, 0.51 mmol) and trans-4-chlorocarbonyl-cyclohexanecarboxylic acid methyl ester (2.10 g, 10.3 mmol) was followed by stirring at room temperature for 18 h. The mixture was partitioned between ethyl acetate (150 ml) and 0.1M aqueous hydrogen chloride solution (100 ml). The layers were separated. The aqueous layer was extracted with two 100-ml portions of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated to dryness. Purification by flash-chromatography with n-heptane/tert-butyl methyl ether as eluent gave the title compound (1.3 g, 46%) as yellow solid. MS m/e: 282 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481528B2
Source datasetuspto-grants-2013_07
ORD IDord-44399cd0819c4b5e856d38932478d58c
Source noteuspto-grants-2013_07