Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10653Generated: October 26, 2026

3-Bromo-4-methoxybenzaldehyde → 4-Methoxy-3-(thiophen-2-yl)benzaldehyde

https://huagongshe.com/reaction/10653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-methoxybenzaldehydeHCID 98662—
Reactant2-Thiopheneboronic acidHCID 2733960—
Product4-Methoxy-3-(thiophen-2-yl)benzaldehydeHCID 2198102496%

Reaction Steps

Ex-41A: 4-Methoxy-3-(thiophen-2-yl)-benzaldehyde was prepared from 3-bromo-4-methoxybenzaldehyde and thiophene-2-boronic acid in a similar manner as described in Ex-3A. Orange oil, 96% yield. 1H-NMR (CDCl3) δ 9.94 (s, 1H), 8.16 (d, J=1.8 Hz, 1H), 7.80 (dd, J=2.4, 8.4 Hz, 1H), 7.57 (dd, J=1.8, 3.6 Hz, 1H), 7.38 (d, J=5.1 Hz, 1H), 7.12 (dd, J=3.6, 5.1 Hz, 1H), 7.09 (d, J=8.4 Hz, 1H), 4.02 (s, 3H). HRMS m/z: calc. 218.0402, found 218.0406.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094801B2
Source datasetuspto-grants-2006_08
ORD IDord-bc3607815f2b4883b3402850fcc9a9b9
Source noteuspto-grants-2006_08