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3-[(3-CHLOROBENZYL)OXY]BENZALDEHYDE synthesis

2synthesis methods
-

Yield:168084-95-5 74%

Reaction Conditions:

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

Steps:

8.1 (1) 3 - (3 - chloryl) benzaldehyde preparation

The 3 - hydroxybenzaldehyde (1.0 g, 8.2 mmol) dissolved in 15 mLDMF in, adding 3 - chlorine animal pen bromine (1.84 g, 9.0 mmol), potassium carbonate (1.35 g, 9.8 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, shall be transparent oil to 1.5 g, yield 74%.

References:

CN107151220,2017,A Location in patent:Paragraph 0178; 0179; 0180; 0181; 0182

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