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1-Bromo-2-(dimethoxymethyl)-4-nitrobenzene synthesis

2synthesis methods
84459-32-5 Synthesis
2-bromo-5-nitrobenzaldehyde

84459-32-5
104 suppliers
$8.00/1g

1-Bromo-2-(dimethoxymethyl)-4-nitrobenzene

115972-68-4
1 suppliers
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Yield:115972-68-4 97%

Reaction Conditions:

with toluene-4-sulfonic acid in methanol; for 8 h;Reflux;

Steps:

A90 Preparation of intermediate 628

In a round bottom flask, 2-bromo-5-nitrobenzene carbaldehyde (29.17g , 0.127 mol), trimethyl orthoformate (2 lmL, 0.192 mol), p-toluenesulfonic acid monohydrate (2.4g 12.6 mmol) were mixed in MeOH (600mL). Then, the reaction mixture was refluxedfor 8 hours. The reaction was cooled down and the solvent was removed. The residue was taken up with water, K2C03 and DCM. The organic layer was separated, dried over MgSO4, filtered and evaporated until dryness to give 34g (97%) of intermediate 628.

References:

WO2017/125530,2017,A1 Location in patent:Page/Page column 343; 344