Synthesis of carbonyl compounds based on the products of addition of polyhaloalkanes to unsaturated systems. Reactions of 1-aryl-5,5-dichloropenta-2,4-dien-1-ones with ethyl acetoacetate

被引:1
作者
Woznesensky, SA
Dudinov, AA
Belenkii, LI
Struchkova, MI
Nesterov, VN
Krayushkin, MM
Struchkov, YT
机构
[1] ND ZELINSKII INST ORGAN CHEM,MOSCOW 117913,RUSSIA
[2] AN NESMEYANOV ORGANOELEMENT CPDS INST,MOSCOW 117813,RUSSIA
关键词
ethyl 4-aryl-6-(2,2-dichlorovinyl)-4-hydroxy-2-oxocyclohexanecarboxylates; synthesis; 1-aryl-5,5-dichloropenta-2,4-dien-1-ones; ethyl acetoacetate; condensation; cyclization; crystal structure; H-1 and C-13 NMR spectra;
D O I
10.1007/BF02495404
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reactions of 1-aryl-5,5-dichloropenta-2,4-dien-1-ones with ethyl acetoacetate in the presence of EtONa give ethyl 4-aryl-6-(2,2-dichlorovinyl)-4-hydroxy-2-oxocyclohexanecarboxylates. The structures of the reaction products were confirmed by H-1 and C-13 NMR spectroscopy and by X-ray diffraction analysis.
引用
收藏
页码:501 / 506
页数:6
相关论文
共 13 条
  • [1] TABLES OF BOND LENGTHS DETERMINED BY X-RAY AND NEUTRON-DIFFRACTION .1. BOND LENGTHS IN ORGANIC-COMPOUNDS
    ALLEN, FH
    KENNARD, O
    WATSON, DG
    BRAMMER, L
    ORPEN, AG
    TAYLOR, R
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1987, (12): : S1 - S19
  • [2] Dudinov AA, 1995, KHIM GETEROTSIKL+, P1511
  • [3] GUNTER H, 1988, NMP SPECTROSCOPY INT
  • [4] IONIN BI, 1983, NMR SPECTROSCOPY ORG, P153
  • [5] LEVY GC, 1972, CARBON 13 NUCLEAR MA
  • [6] NEGREBETSKII VV, 1993, ZH OBSHCH KHIM+, V63, P1374
  • [7] ORLOVA NI, 1992, ZH ORG KHIM, V27, P1289
  • [8] Reichardt C. R. C., 1988, SOLVENTS SOLVENT EFF
  • [9] ROBINSON W, 1988, CRYSTALLOGRAPHIC COM, P366
  • [10] SHAPETKO NN, 1981, TEOR EKSP KHIM, V17, P186