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DOI: 10.1055/s-0030-1258501
Thermal Retro-Aldol Reaction Using Fluorous Ether F-626 as a Reaction Medium
Publication History
Publication Date:
16 July 2010 (online)

Abstract
A high-boiling, fluorous-organic hybrid ether, F-626, was tested for use in thermal retro-aldol reactions and found to be an excellent reaction medium in view of the ease of separation from the product by fluorous/organic biphasic treatment. The recovered F-626 can be readily reused for subsequent runs.
Key words
retro-aldol reaction - fluorous ether - F-626 - biphasic system
-
1a
Green Reaction Media in Organic Synthesis
Mikami K. Blackwell Publishing; Oxford: 2005. -
1b
Green Separation
Processes: Fundamentals and Applications
Afonso CAM.Crespo JG. Wiley-VCH; Weinheim: 2005. - For reviews on fluorous chemistry, see:
-
2a
Handbook
of Fluorous Chemistry
Gladysz JA.Curran DP.Horváth IT. Wiley-VCH; Weinheim: 2004. -
2b For a thematic issue
on fluorous chemistry, see:
Gladysz JA.Curran DP. Tetrahedron 2002. 58: p.3823 -
2c
Ryu I.Matsubara H.Emnet C.Gladysz JA.Takeuchi S.Nakamura Y.Curran DP. In Green Reaction Media in Organic SynthesisMikami K. Blackwell Publishing; Oxford: 2005. p.59 -
2d
Matsubara H.Ryu I. In Green Separation Processes: Fundamentals and ApplicationsAfonso CAM.Crespo JG. Wiley-VCH; Weinheim: 2005. p.219 -
3a
Fujii Y,Tamura E,Yano S, andFurugaki H. inventors; US Patent 6,060,626. -
3b
Fujii Y.Furugaki H.Yano S.Kita K. Chem. Lett. 2000, 926 -
3c
Fujii Y.Furugaki H.Tamura E.Yano S.Kita K. Bull. Chem. Soc. Jpn. 2005, 78: 456 -
4a
Matsubara H.Yasuda S.Sugiyama H.Ryu I.Fujii Y.Kita K. Tetrahedron 2002, 58: 4071 -
4b
Fukuyama T.Arai M.Matsubara H.Ryu I. J. Org. Chem. 2004, 69: 8105 - 5
Chu Q.Yu MS.Curran DP. Tetrahedron 2007, 63: 9890 -
6a
Smith GG.Yates BL. J. Org. Chem. 1965, 30: 2067 -
6b
Yates BL.Quijano J. J. Org. Chem. 1969, 34: 2506 -
6c
Westley JW.Evans RH.Pruess DL.Stempel A. Chem. Soc. D. 1970, 1467 -
6d
Yates BL.Ramirez A.Velasquez O. J. Org. Chem. 1971, 36: 3579 -
6e
Ireland RE.Anderson RC.Badoud R.Fitzsimmons BJ.McGarvey GJ.Thaisrivongs S.Wilcox CS. J. Am. Chem. Soc. 1983, 105: 1988 -
6f
Yoshioka M.Arai M.Nishizawa K.Hasegawa T. J. Chem. Soc., Chem. Commun. 1990, 374 -
7a
Granberg KL.Edvinsson KM.Nilsson K. Tetrahedron Lett. 1999, 40: 755 -
7b
Oikawa H.Oikawa M.Ichihara A.Ubukata M.Isono K. Biosci., Biotechnol., Biochem. 1994, 58: 1933 -
7c
Oikawa M.Ueno T.Oikawa H.Ichihara A. J. Org. Chem. 1995, 60: 5048 -
7d
Kocienski PJ.Brown RCD.Pommier A.Procter M.Schmidt B. J. Chem. Soc., Perkin Trans. 1 1998, 9 -
7e
Horita K.Nagato S.Oikawa Y.Yonemitsu O. Chem. Pharm. Bull. 1989, 37: 1726 -
7f
Wells JL.Bordner J.Bowles P.McFarland JW. J. Med. Chem. 1988, 31: 274 - 9
Doi T.Fukuyama T.Minamino S.Husson G.Ryu I. Chem. Commun. 2006, 1875 - 10
Doi T.Fukuyama T.Minamino S.Ryu I. Synlett 2006, 3013 - 11
Denichoux A.Fukuyama T.Doi T.Horiguchi J.Ryu I. Org. Lett. 2010, 12: 1
References and Notes
General procedure for retro-aldol reactions using F-626: α-Hydroxymethyl ketone 1a (0.5 mmol, 104.7 mg) and F-626 (4 mL, 5.64 g) were placed in a 5 mL two-necked round-bottom flask, and heated at 200 ˚C for 4 h under nitrogen. After cooling to room temperature, the reaction mixture was poured into a separation funnel, and MeCN (4 mL) was added. The MeCN layer was separated, and extracted with FC-72 (6 × 0.33 mL). The combined fluorous layers were evaporated to give F-626 (5.53 g, 98%). The crude reaction mixture obtained from the MeCN layer was purified by silica gel chromatography (hexane-EtOAc, 98:2) to give a mixture of 2a and 3a (87.6 mg; 2a/3a = 95:5)
12To a 5 mL two-necked flask, RuHCl(CO)(PPh3)3 (0.05 mmol, 48.1 mg), benzene (3 mL) and 2-hexene-1-ol (1 mmol, 101.1 mg) were added, and the resulting mixture was heated at 80 ˚C for 10 h under nitrogen. After cooling to room temperature, the solvent was removed under reduced pressure, F-626 (4 mL) was added and the mixture was heated at 200 ˚C for 4 h. Biphasic workup using MeCN and FC-72, followed by purification using silica gel chroma-tography (hexane-EtOAc, 98:2) gave a mixture of 2g and 3g (51 mg; 2g/3g = 96:4)