Cyclobut‐2‐enones from Alkynes via Dichlorocyclobut‐2‐enones
1987; Wiley; Volume: 70; Issue: 2 Linguagem: Inglês
10.1002/hlca.19870700208
ISSN1522-2675
AutoresAdrian A. Ammann, Max Rey, Aǹdré S. Dreiding,
Tópico(s)Cyclopropane Reaction Mechanisms
ResumoAbstract The [2 + 2]‐cycloaddition of dichloroketene (prepared in situ from CCl 3 COCl and Zn(Cu)) with three alkynes 1a–c to form 2,3‐dimethyl‐( 2a ), 2,3‐diethyl‐( 2b ) and 3‐butyl‐4,4‐dichlorocyclobut‐2‐enone ( 2c ) proceeds rapidly in the absence of POCl 3 . The primary products 2a–c rearrange in situ to the 2,4‐dichlorocyclobut‐2‐enones 3a–c under the influence of ZnCL 2 produced during the reaction. ZnCl 2 converts both 2a and 3a into a 4:6 equilibrium mixture of the two; this isomerization does not occur with LiCl. The Cl‐atoms of both 2a , b and 3a , b and of 2c may reductively be removed with Zn(Cu) in AcOH/pyridine to afford the alkylcyclobutenones 4a‐c . Without pyridine, this reduction gives ca. 1:1 mixtures of the double‐bond isomers 4 and 5 in low yields. The cyclobutenones 2c and 4c may be deuterated by CD 3 COOD in the presence of pyridine. D ‐Atom is introduced into 2c at C(4) and at C(γ), and into 4c at C(2) and C(4). A mechanism for this deuteration is considered, which does not involve a cyclobutadienolate 7 , but rather a cyclobutenolate of type 8 . The reductions of 2 and 3 to 4 might also pass through the same type of intermediate 8 .
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