Recently I am researching about FRIEDEL-CRAFTS ACYLATION; ALKYL SIDE-CHAINS; AROMATIC-SUBSTITUTION; UNSTRAINED CYCLOALKANOLS; ARYL; TIN; MECHANISM; FACILE; LENGTH; ALCL3, Saw an article supported by the School of Chemistry at The University of SydneyUniversity of Sydney; Macquarie University; Australian GovernmentAustralian GovernmentCGIAR. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Roemer, M; Keaveney, ST; Proschogo, N. The CAS is 92-86-4. Through research, I have a further understanding and discovery of 4,4′-Dibromobiphenyl. Recommanded Product: 92-86-4
This paper describes the facile synthesis of haloaryl compounds with long-chain alkanoyl substituents by the destannylative acylation of haloaryls bearing tri-n-butyltin (Bu3Sn) substituents. The method allows the synthesis of many important synthons for novel functional materials in a highly efficient manner. The halo-tri-n-butyltin benzenes are obtained by the lithium-halogen exchange of commercially available bis-haloarenes and the subsequent reaction with Bu3SnCl. Under typical Friedel-Crafts conditions, i.e., the presence of an acid chloride and AlCl3, the haloaryls are acylated through destannylation. The reactions proceed fast (<5 min) at low temperatures and thus are compatible with aromatic halogen substituents. Furthermore, the method is applicable to para-, meta-, and ortho-substitution and larger systems, as demonstrated for biphenyls. The generated tin byproducts were efficiently removed by trapping with silica/KF filtration, and most long-chain haloaryls were obtained chromatography-free. Molecular structures of several products were determined by X-ray single-crystal diffraction, and the crystal packing was investigated by mapping Hirshfeld surfaces onto individual molecules. A feasible reaction mechanism for the destannylative acylation reaction is proposed and supported through density functional theory (DFT) calculations. DFT results in combination with NMR-scale control experiments unambiguously demonstrate the importance of the tin substituent as a leaving group, which enables the acylation. Recommanded Product: 92-86-4. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Roemer, M; Keaveney, ST; Proschogo, N or concate me.
Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem