FIELD: organic chemistry and technology. SUBSTANCE: product: compounds of the general formula (I) where: R1= - hydrogen or halogen atom, C1-C6-alkyl, C1-C6-alkoxy or nitro-group; R2 - hydrogen or halogen atom or allyl; R3= - hydrogen atom, C1-C6-alkyl, C1-C6-alkoxy, di-(C1-C6)-alkylamino or nitro-group; R4 - halogen atom; R5, R6-C1-C6-alkyl.Methodofsynthesisinvolvesinteractionof2-R4-5,5--R5, R6-cyclohexene-1,3-diones with salicylic aldehyde or its substituted derivatives in the presence of perchloric acid and triethyl-ortho-formate. Given: N; R1, R2, R3, R4, R5, R6; yield (%); m. p. (C); UV-spectrum (L max - E, nm): 1a; H, H, H, Br; CH3; CH3; 55.1; 308-310; 548.2-33.51. 1b; CH3,, H, H, Br; CH3,; CH3;; 43.6; 305-307; 555.6-82.78. 1c; H, CH3,, CH3,, Br; CH3; CH3;; 41.0; 303-305; 563.1-40.11. 1d; OCH3, H, H, Br; CH3,; CH3;; 53.5; 307-309; 573.4-85.61. 1e; NO2,, H, H, Br; CH3,; CH3;; 54.5; 342-344; 548.2-57.57. 1f; Cl, H, H, Br; CH3; CH3; 51.8; 322-324; 553.1-87.65; 1g; Br, H, H, Br; CH3,; CH3; 63.2; 301-304; 555.6-102.17. 1h; Br, Br, H, Br; CH3,; CH3;; 69.0; 341-343; 558.0-44.92. 1i; Br, Br, OCH3,, Br; CH3,; CH3;; 42.5; 345-347; 573.4-113.65. 1j; H, CH2OH=CH2,, H, Br; CH3,; CH3;; 87.2; 219-220; 550.7-105.13. 1k; CH3,, H, NO2,, Br; CH3,; CH3;; 45.7; 348-350; 553.1-90.34. 1l; H, H, N(CH3)2, Br; CH3,; CH3;; 41.4; 318-320; 698.3-81.72. Synthesized compounds exhibit high spectral properties and can be used as fluorescent dyes for anion-modified fibers and films staining. EFFECT: improved method of synthesis, enhanced quality and properties. 2 cl, 2 tbl
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Authors
Dates
1997-07-20—Published
1995-05-18—Filed