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49781-48-8

2,2-DIFLUOROPROPIONAMIDE synthesis

2synthesis methods
-

Yield:49781-48-8 80.8%

Reaction Conditions:

with ammonia in methanol at 20;Inert atmosphere;Heating;

Steps:

2 Example 2 Preparation of 5,5-difluoro-4-oxo-trans-2-hexenal

The synthetic route of the compound 5,5-difluoro-4-oxo-trans-2-hexenal in the present invention is shown in Figure 3. In a 100mL three-necked flask, add 2g (18.18mmol) of 2,2-difluoropropionic acid and 30mL of dry methanol solution, replace the air in the three-necked flask with nitrogen, pass in ammonia gas and amination reaction for 24h. The reaction temperature is room temperature. 1.6 g of 2,2-difluoropropionamide was produced with a yield of 80.8%.1.6 g (14.68mmol) of 2,2-difluoropropionamide was dissolved in 25mL of toluene solution and dehydrated into 2,2-difluoropropionitrile in the presence of P2O5. 3,3-difluoro-2-butanone can be synthesized by hydrolyzing the generated 2,2-difluoropropionitrile with methylmagnesium iodide, with a yield of 73.6%.

References:

CN112094181,2020,A Location in patent:Paragraph 0028-0030

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