Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List URAZOLE

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

URAZOLE Related Search: