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ChemicalBook CAS DataBase List 3(2H)-Pyridazinone
504-30-3

3(2H)-Pyridazinone synthesis

9synthesis methods
-

Yield:504-30-3 88.9%

Reaction Conditions:

Stage #1: mucochloric acidwith tert-butylhydrazine in water;toluene at 23; for 2.8 h;
Stage #2: with tetrabutylammomium bromide;titanium(IV) oxide in water;toluene at 20; for 4.6 h;Temperature;

Steps:

1-10 Example 9

Add 50g furochloric acid and 9g toluene into a four-necked flask. Under stirring, 23 °C slowly drop a 20% aqueous solution of tert-butylhydrazine (28.4g of tert-butylhydrazine). After the addition, keep it warm for 2.8 h. Add 3.5g of C-TiO2 solid acid and 2.5g of tetrabutylammonium bromide, control the reaction temperature at 20 °C and react for 4.6 h. After the reaction is over, the solid acid catalyst is filtered out and reused. The filtrate was left standing to separate the organic phase and the inorganic phase, and the organic layer was decompressed to recover the solvent toluene to obtain the product pyridazinone. The calculated yield was 88.9%, and the product purity was 96.8% analyzed.

References:

CN112552241,2021,A Location in patent:Paragraph 0022-0031

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