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3-[(2-methoxyphenyl)methoxy]benzaldehyde synthesis

2synthesis methods
-

Yield:123926-42-1 76.7%

Reaction Conditions:

with potassium carbonate in N,N-dimethyl-formamide at 80; for 3 h;

Steps:

18.1 (1) 3 - (2 - methoxy animal pen oxygen radical) benzaldehyde preparation

The 3 - hydroxybenzaldehyde (0.50 g, 4 . 14 mmol) dissolved in 8 ml DMF in, adding 2 - methoxy animal pen bromine (1.00 g, 4 . 97 mmol), potassium carbonate (0.86 g, 6 . 22 mmol), 80 °C reaction 3 hours, adding 15 ml distilled water, extracted with ethyl acetate twice (2 × 20 ml), then saturated sodium chloride solution for washing 1 time, dried with anhydrous sodium sulfate. Concentrated, column chromatography, eluting agent is petroleum ether: ethyl acetate=3:1, to obtain white solid 0.76 g, yield 76.7%

References:

CN107151220,2017,A Location in patent:Paragraph 0343; 0344; 0345; 0346; 0347