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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593452Generated: October 28, 2026

2-Bromopyridine → 2-Nitro-4-(2-pyridinyl)benzaldehyde

https://huagongshe.com/reaction/593452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant2-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehydeHCID 75487512—
Solvent1,4-DioxaneHCID 31275—
Product2-Nitro-4-(2-pyridinyl)benzaldehydeHCID 86653480—

Reaction Steps

The title compound was prepared by the procedure as described in Example 101 (Step C) using 2-nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde and 2-bromopyridine in dioxane (reflux).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242964B2
Source datasetuspto-grants-2016_01
ORD IDord-807e4c183e4b45a689b76ea445f0bba1
Source noteuspto-grants-2016_01