Certain features of the reductive cyclization of compounds with a CCl2 grouping |
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Authors: | R Kh Freidlina A A Kamyshova L A Zhuravleva E Ts Chukovskaya |
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Institution: | 1. Institute of Heteroorganic Compounds, Academy of Sciences of the USSR, Moscow
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Abstract: | 1. |
Reductive cyclization of compounds with the CCl2 grouping, ClCH2CH2CCl2CH2CClXR (R=H, CH3; X=CN, CO2CH3) led to the formation of monosubstituted cyclopropanes, cyclo-C3H5CH2CHXR. Under the reaction conditions, the Cl atom in the position to CO2CH3 and CN groups is reduced without taking part in cyclization.
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The presence of chloro-substituted C atoms in the direction to the CCl2CH2CHC1 fragment hinders the reductive cyclization of this fragment.
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Cyclization by means of the two dichloromethyl groups in the compound CHC12CH2CHC12 does not take place. In this case, the principal reaction route is a stepwise reduction and alkoxylation.
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