Platinum/tin catalyzed hydroformylation of naturally occurring monoterpenes

Citation
Ev. Gusevskaya et al., Platinum/tin catalyzed hydroformylation of naturally occurring monoterpenes, J MOL CAT A, 152(1-2), 2000, pp. 15-24
Citations number
37
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
ISSN journal
13811169 → ACNP
Volume
152
Issue
1-2
Year of publication
2000
Pages
15 - 24
Database
ISI
SICI code
1381-1169(20000301)152:1-2<15:PCHONO>2.0.ZU;2-G
Abstract
(-)-beta-Pinene, R-(+)-limonene, and (-)-camphene have been hydroformylated regiospecifically to give exclusively the linear isomers Of corresponding aldehydes. The following systems were used as catalysts: PtCl2(PPh3)(2)/SnC l2/PPh3, and PtCl2(diphosphine)/SnCl2/PPh3 whose diphosphines were 1,2-bis( diphenylphosphino)ethane, 1,3-bis(diphenylphosphino)propane and 1,4-bis(dip henylphosphino) butane. The hydroformylation of beta-pinene yields trans-10 -formylpinane with a 98% diastereoisomeric excess (d.e.), while limonene an d camphene give the diastereoisomers of the corresponding aldehydes in appr oximately equal amounts (d.e. of ca. 10 and 15%, respectively). Differently from most of the rhodium and cobalt catalysts, the undesirable isomerizati on of beta- to alpha-pinene is rather slow (1-5% based on reacted beta-pine ne). The primarily formed aldehyde of limonene undergoes the highly diaster oselective intramolecular cyclization (d.e. of virtually 100%) catalyzed by the platinum/tin active species yielding 4,8-dimethyl-bicyclo[3.3.1]non-7- en-2-ol. The effects of the catalyst composition and ligand nature on the p roduct distribution have been studied. The use of PPh3 as the only phosphor ous-containing ligand, as well as the excess of SnCl2 (Sn/Pt > 1) promote t he isomerizations of monoterpenes. The system with 1,3-bis(diphenylphosphin o)propane causes excessive hydrogenation of the olefinic double bonds. Unde r optimized conditions, chemoselectivities for aldehyde formation of near 9 0% have been attained for all monoterpenes studied. (C) 2000 Elsevier Scien ce B.V. All rights reserved.