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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970997Generated: October 29, 2026

1-Bromo-3,5-dimethoxybenzene → (3,5-Dimethoxy-phenyl)-(4-methoxy-3-nitro-phenyl)-methanol

https://huagongshe.com/reaction/970997

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3,5-dimethoxybenzeneHCID 639187—
Reactant4-Methoxy-3-nitrobenzaldehydeHCID 700608—
ReactantMagnesiumHCID 5462224—
Reactant3-(4-Methoxy-3-nitro-phenyl)-(3,4-dimethoxy-phenyl)-methanolHCID 69205655—
Product(3,5-Dimethoxy-phenyl)-(4-methoxy-3-nitro-phenyl)-methanolHCID 6920258760%

Reaction Steps

(4-Methoxy-3-nitro-phenyl)-(3,5-dimethoxy-phenyl)-methanol was prepared analogously to 3-(4-methoxy-3-nitro-phenyl)-(3,4-dimethoxy-phenyl)-methanol using 3,5-dimethoxy-bromobenzene (5.0 g, 23.0 mmol), magnesium turning (0.6 g, 23.0 mmol) and 4-methoxy-3-nitro-benzaldehyde (3.5 g, 19.2 mmol). The crude product was purified by flash chromatography (silica gel, Hexane:EtOAc 1:1) to afford (4-methoxy-3-nitro-phenyl)-(3,5-dimethoxy-phenyl)-methanol (3.7 g, 60%) as an oil: 1H NMR (CDCl3) δ 7.88 (s, 1H), 7.54-7.50 (dd, J=2, 8 Hz, 1H), 7.04 (d, J=8 Hz, 1H), 6.38 (d, J=1 Hz, 1H), 5.72 (d, J=3 Hz, 1H), 3.93 (s, 3H), 3.76 (s, 6H), 2.45 (d, 2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312241B2
Source datasetuspto-grants-2007_12
ORD IDord-d8ab7f30f44a410c8c29031d3e1925b7
Source noteuspto-grants-2007_12