FIELD: organic chemistry. SUBSTANCE: product of the general formula RNHC/O/-N/R1R2/ where R - phenyl unsubstituted or substituted with a single or multihalide atoms, lower alkyl, lower alkoxy- arylhydroxy-group, trifluoromethyl, unsubstituted or once substituted with lower alkoxy-group, benzthiazolyl- or benzoxazolyl-group; R1,R2 - hydrogen or lower alkyl but R1 and R2 can not simultaneously mean hydrogen atom. Reagent 1: urea of formula (II) H2N-C(O)-N(R1R2) where R1,R2 - as indicated above. Reagent 2: aromatic amine (III) of the formula RNH2 and formula (IV) . Reaction conditions: process is carried out at 130-250 C in the presence of amine of formula (III) at the molar ratio of urea (II) to amine (III) and amine (IV) = 1:(0.5-0.7):(2-15). Method is used for synthesis of semiproducts used for synthesis of pyrethroids. EFFECT: improved method of synthesis.
Title | Year | Author | Number |
---|---|---|---|
HERBICIDE AGENT AND A METHOD FOR STRUGGLE AGAINST WEEDS | 1991 |
|
RU2054871C1 |
PROCESS FOR PREPARING ISOCYANIC ACID IN STABLE FORM READY FOR USE | 1990 |
|
RU2015945C1 |
METHOD OF OBTAINING N-FENYL-N',N'-DIALKYLUREA | 1982 |
|
SU1135152A1 |
METHOD OF PRODUCNG DERIVATIVES OF N-(MONO- OR DISUBSTITUTED)-N-ARYLUREAS | 0 |
|
SU1246891A3 |
PROCESS OF PRODUCTION OF NON-SYMMETRICALLY SUBSTITUTED UREAS OF CARBAMATES OR THIOCARBAMATES OR SUBSTITUTED ISOCYANATES | 0 |
|
SU1831474A3 |
METHOD OF SYNTHESIS OF PHENYLUREA | 0 |
|
SU685146A3 |
METHOD OF OBTAINING PHENOXYPROPYLAMINE DERIVATIVES OR SALTS THEREOF | 0 |
|
SU612621A3 |
0 |
|
SU308574A1 | |
TETRAZOLE DERIVATIVES, METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION SHOWING PROPERTY OF ANTAGONIST OF ANGIOTENSIN-II RECEPTORS | 1992 |
|
RU2078764C1 |
METHOD OF OBTAINING PHENOXYPROPYLAMINE DERIVATIVES OR SALTS THEREOF | 0 |
|
SU619099A3 |
Authors
Dates
1994-10-15—Published
1991-02-28—Filed