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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466164Generated: October 30, 2026

4-Chlorobenzoyl chloride → 6-Benzoyloxy-2-(4-chlorobenzoyloxy)-3-cyanopyridine

https://huagongshe.com/reaction/466164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantHCID 178510098HCID 178510098—
Product6-Benzoyloxy-2-(4-chlorobenzoyloxy)-3-cyanopyridineHCID 1404964082.8%

Reaction Steps

The general procedure of Example 90 was followed using 1.00 g of 6-benzoyloxy-3-cyano-2-hydroxypyridine and 0.72 g of 4-chlorobenzoyl chloride, thereby producing 1.29 g of the title compound in a yield of 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155113
Source datasetuspto-grants-1992_10
ORD IDord-7b2285d5154e4db49587bf58fb462ac1
Source noteuspto-grants-1992_10