The electrophilic substitution of benzocyclobutene—II: Benzoylation, sulphonation, bromination and chlorination
JBF Lloyd, PA Ongley
Index: Lloyd,J.B.F.; Ongley,P.A. Tetrahedron, 1965 , vol. 21, p. 245 - 254
Full Text: HTML
Citation Number: 30
Abstract
Benzoylation of benzocyclobutene gives β-phenethyl chloride, 2′-(2-chloroethyl)- benzophenone and 4-benzoylbenzocyclobutene in proportions dependent on solvent and catalyst; β-phenethyl chloride gives no discrete benzoylation product under conditions where benzocyclobutene gives large quantities of the chloroethylbenzophenone. Sulphonation, using dioxan-sulphur trioxide complex, gives β-hydroxyethyl-benzene-o- ...
Related Articles:
5??HT radioligands for human brain imaging with PET and SPECT
[Blanckaert; Vandecapelle; Staelens; Burvenich; Dierckx; Slegers Journal of Labelled Compounds and Radiopharmaceuticals, 2004 , vol. 47, # 9 p. 591 - 598]
[Carr, Damien J.; Kudavalli, Jaya Satyanarayana; Dunne, Katherine S.; Mueller-Bunz, Helge; Gilheany, Declan G. Journal of Organic Chemistry, 2013 , vol. 78, # 20 p. 10500 - 10505]
[Adamczyk, Maciej; Watt, David S.; Netzel, Daniel A. Journal of Organic Chemistry, 1984 , vol. 49, # 22 p. 4226 - 4237]
[Adamczyk, Maciej; Watt, David S.; Netzel, Daniel A. Journal of Organic Chemistry, 1984 , vol. 49, # 22 p. 4226 - 4237]
[Ponton, John; Helquist, Paul; Conrad, Preston C.; Fuchs, Philip L. Journal of Organic Chemistry, 1981 , vol. 46, # 1 p. 118 - 122]