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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799158Generated: November 1, 2026

p-Bromochlorobenzene → (4-Chlorophenyl)(6-chloro-3-pyridinyl)methanone

https://huagongshe.com/reaction/1799158

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
Reactant6-Chloro-N-methoxy-N-methylnicotinamideHCID 11435597—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4-Chlorophenyl)(6-chloro-3-pyridinyl)methanoneHCID 2014573179%

Reaction Steps

To a solution of 4-chlorobromobenzene (33.88 g, 177 mmol) in THF (200 mL), a solution of BuLi (118 mL, 142 mmol, 1.2 M solution in hexane) was added at −78° C. The mixture was stirred for 1 h and a solution of compound A (23.6 g, 118 mmol) in THF (100 mL) was added to it dropwise. The mixture was stirred for additional 1 h, quenched with saturated NH4Cl solution and extracted with ethyl acetate (300 mL). The organic layer was dried (Na2SO4), filtered and evaporated. The crude product was purified using column chromatography to obtain 23.4 g (79%) of compound B as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343996B2
Source datasetuspto-grants-2013_01
ORD IDord-63a43f72efaa48f1acde52507e31ebc2
Source noteuspto-grants-2013_01