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ChemicalBook CAS DataBase List URAZOLE
3232-84-6

URAZOLE synthesis

11synthesis methods
-

Yield: 89%

Reaction Conditions:

in water;acetone

Steps:

5 EXAMPLE 5
EXAMPLE 5 400 g of N-methyl-pyrrolidone and 160 g of hydrazodicarbonamide still moist from the suction filter (contains 73.8% of dry hydrazodicarbonamide) are heated to 205° C. in a one-liter stirrer apparatus similar to that of Example 1. The ammonia which begins to be released at 160° C. is expelled with nitrogen. After a reaction time of 3.5 hours at 205° C., about 300 g of solvent are distilled off in a water jet vacuum and acetone is added to the solution remaining behind. Triazolidine-3,5-dione which crystallises out is suction-filtered after it has cooled to room temperature and is then washed with acetone and dried. 74 g of a 97.5% pure 1,2,4-triazolidine-3,5-dione are obtained. A further 16 g of a 96.5% 1,2,4-triazolidine-3,5-dione can be isolated from the mother liquor, so that the total yield is 90 g (89% of the theoretical yield).

References:

Bayer Aktiengesellschaft US4323687, 1982, A

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