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WEI Jie-Ping He-Ping ZENG Dan-Feng XU Jian KIU, . The formation of 1,1-diacetate derivativeJ. Journal of South China Normal University (Natural Science Edition), 2009, 1(1): 71-76 .
Citation: WEI Jie-Ping He-Ping ZENG Dan-Feng XU Jian KIU, . The formation of 1,1-diacetate derivativeJ. Journal of South China Normal University (Natural Science Edition), 2009, 1(1): 71-76 .

The formation of 1,1-diacetate derivative

  • Abstract Three new compounds 1, 2 and 3 have been synthesized by Perkin-type condensation reaction. The crystal structures of compounds 1 and 2 were determined by X-ray single crystal diffraction. The experimental results show the following results. The compound 1, (E)-2-2'-(1''-acetyl-1H-indol-3''-yl)vinyl-quinolin-8-yl acetate, belongs to the monoclinic, space group P2(1)/c with unit cell parameters a=2.26566(9) nm, b=2.01990(8) nm, c=0.79445(3) nm, =90, =90.715(2) , =90, V=3.6354(2) nm3, Z=8, Dc=1.353 Mg/m3, =0.091 mm-1, F(000)=1552, R1=0.0526 and wR2=0.1409. The compound 2, 1,1-Diacetoxy-1-(3'-benzo bthinophene)methane, belongs to the orthorhombic, space group Pccn with with unit cell parameters a=1.70116(8) nm, b=2.00171(8) nm, c=0.76628(3) nm, =90, =90, =90, V=2.60936(19) nm3, Z=8, Dc=1.345 Mg/m3, =0.251 mm-1, F(000)=1104, R1=0.0342 and wR2=0.0985. The formation of compounds 1,2 and 3 show that the acidity in the Perkin type reaction will result in 1,1-diacetate formation and reduce the yield of condensation products.
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