Synthesis of meta-substituted monodentate phosphinite ligands and implication in hydroformylation
Title | Synthesis of meta-substituted monodentate phosphinite ligands and implication in hydroformylation |
Publication Type | Journal Article |
Year of Publication | 2017 |
Authors | Deshmukh, SS, Gaikwad, SR, Pandey, S, Mali, PS, Chikkali, SH |
Journal | Journal of Chemical Sciences |
Volume | 129 |
Issue | 8 |
Pagination | 1143-1152 |
Date Published | AUG |
Type of Article | Article |
Abstract | Synthesis of meta-substituted phosphinite ligands 3,3'-(methoxyphosphanediyl) bis(N, N-diethylaniline) (4a) and methoxybis(3-methoxyphenyl) phosphane (4b), in high yields, has been demonstrated. Typical phosphorus chemical shift between 110-120 ppm, appearance of methoxy protons and corresponding carbon, as well as ESI-MS spectra unambiguously confirmed the existence of phosphinite ligands 4a and 4b. To demonstrate the synthetic usefulness of 4a and 4b, these ligands were tested in the rhodium catalyzed hydroformylation of 1-octene. The diethylamine substituted ligand 4a was found to be highly active, whereas 4bwas less reactive but revealed slightly better regioselectivity of 62% under optimized conditions. Additionally, 4a and 4b were found to catalyze the hydroformylation of styrene, 1-undecenol and 1,1-disubstituted functional olefin, methyl methacrylate. Both the ligands displayed excellent conversion of styrene, and 4b revealed an excellent branch selectivity of 75%. Although 1-undecenol proved to be amenable to hydroformylation (85-90% conversion to aldehyde), both the ligands failed to discriminate between the linear and branched products. Substrate methyl methacrylate proved to be highly challenging and reduced conversion (between 33-42%) was observed under optimized conditions. Ligand 4a was found to be highly selective towards linear aldehyde (81% linear selectivity). |
DOI | 10.1007/s12039-017-1341-z |
Type of Journal (Indian or Foreign) | Indian |
Impact Factor (IF) | 1.085 |
Divison category:
Central NMR Facility
Polymer Science & Engineering
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