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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10726Generated: October 26, 2026

5-Bromo-2,4-dimethoxybenzaldehyde → 2,4-Dimethoxy-5-pyridin-3-yl-benzaldehyde

https://huagongshe.com/reaction/10726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2,4-dimethoxybenzaldehydeHCID 668346—
Reactant3-Pyridinylboronic acidHCID 2734378—
Product2,4-Dimethoxy-5-pyridin-3-yl-benzaldehydeHCID 2198111368%

Reaction Steps

Ex-104A: 2,4-Dimethoxy-5-pyridin-3-yl-benzaldehyde was prepared in a similar manner as described in Ex-3A from pyridine-3-boronic acid and 5-bromo-2,4-dimethoxybenzaldehyde, 68% yield. 1H-NMR (CDCl3) δ 10.33 (s, 1H), 8.71 (d, J=1 Hz, 1H), 8.51–8.53 (m, 1H), 7.81 (s, 1H), 7.74–7.78 (m, 1H), 7.27–7.31 (m, 1H), 6.52 (s, 1H), 3.99 (s, 3H), 3.91 (s, 3H). HMRS (EI) calcd. for C14H13NO3: 243.0895; found: 243.0888.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094801B2
Source datasetuspto-grants-2006_08
ORD IDord-fd3f66696ce2493987252185d90a7bbb
Source noteuspto-grants-2006_08