Dibenzocyclooctane carboxylic ether compounds with herbicidal activity
A technology of ester compounds and cyclooctane, which is applied in the directions of organic chemistry, animal repellent, plant growth regulator, etc., can solve the problems of unpublished bicarboxy ester compounds and so on.
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[0124] Synthesis of Compound 9 in Table 1:
[0125]
[0126] Drop into II (7.5 grams, 0.0335mol), dichloromethane (70ml), oxalyl chloride (6.4 grams, 0.0503mol) in the reaction bottle of 150ml, absorb tail gas with lye, react at room temperature for 30 minutes, add 2 drops of DMF, and A large amount of gas was released, and the reaction was stopped after 2 hours. The reaction liquid was concentrated under reduced pressure to obtain 5.6 g of oily substance II-1.
[0127]
[0128] Add II-1 (1.0 grams, 0.00365mol) and 10ml of dichloromethane in a 50ml reaction flask, add ethylene glycol (2.2 grams, 0.0365mol) after stirring, triethylamine (0.44 grams, 0.00365mol), room temperature React for 2 hours. Pour the reaction solution into a 250ml separatory funnel, add 100ml ethyl acetate, 50ml water, separate layers, wash the ethyl acetate layer with 50ml saturated aqueous sodium bicarbonate solution, 50ml saturated aqueous sodium chloride solution, and dry over anhydrous magnesi...
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