PLANAR CHIRAL SYSTEMS .4. AN EFFICIENT ROUTE FOR THE PREPARATION OF 5-FORMYL-4-HYDROXY[2.2]PARACYCLOPHANE (FHPC)

Authors
Citation
H. Hopf et Dg. Barrett, PLANAR CHIRAL SYSTEMS .4. AN EFFICIENT ROUTE FOR THE PREPARATION OF 5-FORMYL-4-HYDROXY[2.2]PARACYCLOPHANE (FHPC), Liebigs Annalen, (2), 1995, pp. 449-451
Citations number
11
Categorie Soggetti
Chemistry
Journal title
ISSN journal
09473440
Issue
2
Year of publication
1995
Pages
449 - 451
Database
ISI
SICI code
0947-3440(1995):2<449:PCS.AE>2.0.ZU;2-U
Abstract
For the preparation of the title compound, 4-hydroxy[2.2]paracyclophan e (1) is first converted to the carbamate 2. Metalation of 2 with sec- butyllithium yields an ortho-anion which after trapping with dimethylf ormamide and acidic work-up provides 6 in 64% yield. Further applicati on of the cyclophane anion include its capture by trimethylsilyl chlor ide to the trimethylsilyl derivative 3 (76%) and its Fries rearrangeme nt to the phenol 4 (78%). The spectroscopic and analytical data of the new compounds are described in full detail.