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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048372Generated: October 27, 2026

Methyl 4-chlorobenzoate → 1-(4-Chlorophenyl)-2-(4-chloropyridin-2-yl)ethanone

https://huagongshe.com/reaction/1048372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-chlorobenzoateHCID 14307—
Reactant4-Chloro-2-methylpyridineHCID 581392—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Chlorophenyl)-2-(4-chloropyridin-2-yl)ethanoneHCID 58573890—

Reaction Steps

To a solution of 4-chloro-2-methylpyridine (23.07 g, 181 mmol) and methyl 4-chlorobenzoate (30.8 g, 181 mmol) in dry THF (500 mL) at 0° C. was added 1 M LiHMDS in THF (63.5 g, 380 mmol) slowly via a dropping funnel. When complete, the reaction was quenched with NaHCO3 solution, concentrated under reduced pressure, and extracted with ethyl acetate. The combined organics were dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-c7bfc25d72f44c019d5bae7b0b78a9e9
Source noteuspto-grants-2013_10