FIELD: organic chemistry. SUBSTANCE: product: N-4-(1-hydroxy- 1-amino)- ethoxy- (carbonyl- 2,2,2-trifluoroethyl-)- phenyl-N- alkyl-N′- (α-naphthyl)-urea of the formula HO-C(CF3)(X)-C6H4-N(R)-CONHR′ where x CONH2, R-C2H5, R1-(CH2)6Cl, tmelt 159-160 C; X CONH2 R=R1CH3,C2H5, tmelt 190 C; X CONH2, R=C2H5, R1=CH3, tmelt 176-177 C; X CONH2, R=C2H5, R1=α-naphthyl, tmelt 200 C (with decomposition and sublimation); X COO-C2H5, R CH3,R1= α-naphthyl, tmelt 115-118 C; X COOC2H5, R iso-C3H7,R1-(CH2)6. Synthesized compound is substance of light-yellow color, dense consistency. The yield of the end product is 67-95% Reagent 1: CH3OCOC(CF3)(OH)-C6H4N(R)-(CONHR1). Reagent 2: ammonia aqueous solution. Reaction conditions: process is carried out at 20-25 C. Synthesized compounds were used in agriculture. EFFECT: improved method of synthesis. 3 tbl
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Authors
Dates
1995-08-27—Published
1991-03-12—Filed