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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51588Generated: October 26, 2026

Phenol → 4-Bromo-2-phenoxybenzaldehyde

https://huagongshe.com/reaction/51588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantReserpineHCID 5770—
Reactant5-Bromo-2-fluorobenzaldehydeHCID 736327—
Reactant2-(3-Bromophenoxy)benzonitrileHCID 28602353—
SolventAcetonitrileHCID 6342—
Product4-Bromo-2-phenoxybenzaldehydeHCID 1641342946%

Reaction Steps

The title compound was prepared in a 46% yield from 5-bromo-2-fluoro-benzaldehyde and phenol in a manner similar to that described for the preparation of 5-bromo-phenoxybenzonitrile: 1H NMR (DMSO-d6, 400 MHz) δ 10.32(s, 1H), 7.92(s, 1H), 7.81(d, 1H), 7.46(t, 2H), 7.27(t, 1H), 7.18(d, 2H), 6.90(d, 1H) RP-HPLC (Hypersil HS, 5 μm, 100 A 4.6×250 mm; 25%-100% acetonitrile—0.05 M ammonium acetate over 10 min, 1 ml/min) tr 13.08 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713474B2
Source datasetuspto-grants-2004_03
ORD IDord-34160c193bba4f8993363aa30d6abc90
Source noteuspto-grants-2004_03