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(3,4-DICHLOROPHENYL)ACETALDEHYDE synthesis

2synthesis methods
-

Yield:93467-56-2 77%

Reaction Conditions:

with Dess-Martin periodane in dichloromethane at 20; for 1.5 h;

Steps:

8

[00125] A mixture of the above material (1.50 g, 7.85 mmol) and DMP (4.0 g, 9.4 mmol) in DCM (40 mL) was stirred at RT for 1.5 h, forming a white suspension. Hexanes (100 mL) was added, and the suspension was filtered through a celite cake. The filtrate was collected and concentrated to dryness under reduced pressure, and the residue was purified on silica gel by flash chromatography (EtOAc/hexanes, 1:6 to 1:4), affording 2-(3,4-dichlorophenyl)acetaldehyde as a pale green liquid (1.15 g, 77%). 1H NMR (400 MHz, CDCl3) δ 9.75 (t, J = 1.9 Hz, 1H), 7.44 (d, J = 8.2 Hz, 1H), 7.32 (d, J = 2.1 Hz, 1H), 7.05 (dd, J = 8.2, 2.1 Hz, 1H), 3.68 (d, J = 1.9 Hz, 2H).

References:

WO2021/224864,2021,A1 Location in patent:Paragraph 00125

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