Subscribe to RSS
DOI: 10.1055/s-2006-939696
Stereocontrolled Copper Iodide Catalyzed Phosphorus-Carbon Bond Formation: An Efficient Synthesis of Scalemic Tertiary Phosphineboranes
Publication History
Publication Date:
24 April 2006 (online)
Abstract
A mild and efficient protocol for P-C bond formation was developed with sub-stoichiometric amounts of copper iodide as a catalyst. A series of sterically and electronically divergent phosphineboranes were subjected to coupling reactions and the corresponding products were obtained in high yields with retention of configuration. The reaction proceeded under non-basic conditions thus avoiding base-catalyzed racemization.
Key words
tertiary phosphineboranes - phosphorylation - ethyl diazoacetate - pseudorotation
-
1a
Fache F.Schultz E.Tommasino L.Lemaire M. Chem. Rev. 2000, 100: 2159 -
1b
Braunstien P.Naud F. Angew. Chem. Int. Ed. 2001, 40: 680 -
1c
Helmchen G.Pfaltz A. Acc. Chem. Res. 2000, 33: 336 -
1d
Pietrusiewicz KM.Zablocka M. Chem. Rev. 1994, 94: 1375 -
2a
Schmidbaur H.Müller G. Monatsh. Chem. 1980, 111: 1233 -
2b
Schmidbaur H.Weiss E. Angew. Chem., Int. Ed. Engl. 1981, 20: 283 -
2c
Schmidbaur H.Müller G.Dash KC.Milewski-Mahrla B. Chem. Ber. 1981, 114: 441 -
2d
Müller G.Neugebauer D.Geike W.Köhler FH.Pebler J.Schmidbaur H. Organometallics 1983, 2: 257 -
2e
Oshiki T.Hikosaka T.Imamoto T. Tetrahedron Lett. 1991, 32: 3371 -
2f
Koide Y.Sakamoto A.Imamoto T. Tetrahedron Lett. 1991, 32: 3375 -
2g
Imamoto T.Matsuo M.Nonomura T.Kishikawa K.Yanagawa M. Heteroat. Chem. 1993, 4: 475 -
2h
Imamoto T.Oshiki T.Onozawa T.Matsuo M.Hikosaka T.Yanagawa M. Heteroat. Chem. 1992, 3: 563 -
3a
Juge S.Stephan M.Laffitte JA.Genet JP. Tetrahedron Lett. 1990, 31: 6357 -
3b
Camus JM.Andrieu J.Richard P.Poli R.Darcel C.Juge S. Tetrahedron: Asymmetry 2004, 15: 2061 -
3c
Corey EJ.Chen Z.Tanoury GJ. J. Am. Chem. Soc. 1994, 115: 11000 -
4a
Oshiki T.Imamoto T. J. Am. Chem. Soc. 1992, 114: 3975 -
4b
Al Masum M.Kumaraswamy G.Livinghouse T. J. Org. Chem. 2000, 68: 4776 -
4c
Pican S.Gaumont AC. Chem. Commun. 2005, 2393 -
4d
Crepy KVL.Imamoto T. Top. Curr. Chem. 2003, 229: 1 -
4e
Katagiri K.Danjo H.Yamaguchi K.Imamoto T. Tetrahedron 2005, 61: 4701 - 5
Wolfe B.Livinghouse T. J. Am. Chem. Soc. 1998, 120: 5116 -
7a
Gelman D.Jiang L.Buchwald SL. Org. Lett. 2003, 5: 2315 -
7b
Suarez A.Fu FC. Angew. Chem. Int. Ed. 2004, 43: 3580 -
7c
Thielges S.Bisseret P.Eustache J. Org. Lett. 2005, 7: 681 - 10
Imamoto T.Oshiki T.Onozaza T.Kusumoto T.Sato K. J. Am. Chem. Soc. 1990, 112: 5244
References and Notes
The reaction was conducted in a wide range of solvents and the isolated yields of product (±)-2 were: CH2Cl2, 15%; CHCl3, 10%; DMF, 25%; THF-DMS, 5%; and HMPA, 12%.
8Other than the phosphineborane, we have also tested diethyl phosphate and ethyl diazoester under similar conditions but no trace of coupled product was detected; only starting material was recovered.
9Absolute stereochemistry was assigned by analogy with compound 10a.
11[( R ) - (Ethoxycarbonylmethyl)phenylmethylphosphino]-borane ( 2a); Typical Procedure A mixture of 1 (138 mg, 1.0 mmol), CuI (9.5 mg, 0.05 mmol, 5 mol%), and diazo compound (136 mg, 1.2 mmol) was dissolved in MeCN and the resulting solution was stirred at ambient temperature. After 3 h, the reaction mixture was quenched with a sat. solution of NH4Cl, and the aqueous layer was extracted with EtOAc. The combined extracts were washed with a sat. solution of NaCl and dried over anhyd Na2SO4. The solvent was evaporated under reduced pressure and the resulting residue was subjected to column chromatography on silica gel (EtOAc-hexane, 2:8) to give (Rp )-2a (212 mg) in 95% yield as a colorless oil; [α]D 25 -5.9 (c 1.0, benzene). 1H NMR (200 MHz, CDCl3): δ = 1.15 (t, J = 6.77 Hz, 3 H), 1.80 (d, 3 J P-H = 10.16 Hz, 3 H), 2.80-2.95 (m, 2 H), 4.00 (q, J = 4.23, 7.6 Hz, 2 H), 7.40-7.55 (m, 3 H), 7.65-7.80 (m, 2 H). MS (70 eV): m/z (%) = 224 (M+, 24).