A kind of synthetic method of 2,4-dichlorophenylacetaldehyde
A technology of dichlorophenylacetaldehyde and a synthesis method, which is applied in the preparation of heterocyclic compounds, organic chemistry, etc., can solve the problems such as the reduction of the content of 2,4-dichlorophenylacetaldehyde, and achieve the improvement of content and yield and cost reduction. , to avoid the effect of side effects
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Embodiment 1
[0025] A kind of synthetic method of 2,4-dichlorophenylacetaldehyde, its concrete steps are:
[0026] (1) Closed loop
[0027] Add 118.9g of sodium methoxide solution (5% mass fraction) to 50ml of methanol, stir evenly, add 17.5g of 2,4-dichlorobenzaldehyde, stir until completely dissolved, then add 14.3g of ethyl acetoacetate dropwise, drop After completion, the reaction was carried out at 60° C., followed by TLC until the reaction was complete. After filtration, the filtrate was cooled to -5° C. for crystallization, and 22.7 g of solid intermediate I was obtained by suction filtration, with a content of 85% and a yield of 87%.
[0028] (2) Alkaline hydrolysis
[0029] Add 34.6g potassium carbonate aqueous solution (mass fraction: 20%) to 13.1g intermediate product I, keep the temperature at 20°C for reaction, TLC tracking detection until the reaction is complete;
[0030] (3) Acid adjustment
[0031] The above-mentioned completely reacted solution was lowered to room temp...
Embodiment 2
[0035] A kind of synthetic method of 2,4-dichlorophenylacetaldehyde, its concrete steps are:
[0036] (1) Closed loop
[0037] Add 907g of sodium ethoxide solution (mass fraction: 15%) to 200ml of ethanol, stir evenly, add 175g of 2,4-dichlorobenzaldehyde, stir until completely dissolved, then add 390g of ethyl acetoacetate dropwise, dropwise, 40 ℃ heat preservation reaction, TLC tracking detection until the reaction is complete, filter, the filtrate is cooled to -5 ℃ for crystallization, suction filtration to obtain 229.8 g of solid intermediate product I, the content is 83%, and the yield is 88%.
[0038] (2) Alkaline hydrolysis
[0039] Add 212.7g of sodium carbonate aqueous solution (5% mass fraction) to 13.1g of intermediate product I, keep the reaction at 40°C, and track and detect by TLC until the reaction is complete;
[0040] (3) Acid adjustment
[0041] The above-mentioned fully reacted solution was lowered to room temperature, acidified with acetic acid until the...
Embodiment 3
[0045] A kind of synthetic method of 2,4-dichlorophenylacetaldehyde, its concrete steps are:
[0046] (1) Closed loop
[0047] Add 123.1g of sodium isopropoxide solution (mass fraction: 10%) to 80ml of isopropanol, stir evenly, add 17.5g of 2,4-dichlorobenzaldehyde, stir until completely dissolved, then add dropwise 26g of ethyl acetoacetate Ester, dripping, 50 ℃ heat preservation reaction, TLC tracking detection until the reaction is complete, filtration, the filtrate cooled to -5 ℃ crystallization, suction filtration to obtain 22.5g of solid intermediate product I, the content is 81%, the yield is 86%.
[0048] (2) Alkaline hydrolysis
[0049] Add 63.2g sodium bicarbonate aqueous solution (mass fraction is 10%) to 13.1g intermediate product I, 30 ℃ of heat preservation reactions, TLC traces and detects until the reaction is complete;
[0050] (3) Acid adjustment
[0051] The above-mentioned fully reacted solution was lowered to room temperature, acidified with hydrochlori...
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