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DOI: 10.1055/s-0030-1259690
Rasta Resin-DMAP and its Use as a Recyclable Catalyst for the Addition of Carbon Dioxide to Epoxides
Publication History
Publication Date:
25 February 2011 (online)
Abstract
Rasta resin-DMAP, a new heterogeneous polystyrene-based amine, has been synthesized and used as a catalyst in addition reactions of carbon dioxide to epoxides to afford cyclic carbonate products. This new material was found to be a more efficient catalyst than divinyl benzene cross-linked polystyrene-supported DMAP, and was readily recovered and reused without significant loss of catalytic activity.
Key words
polymer-supported organocatalyst - polystyrene - DMAP - carbon dioxide - cyclic carbonate
- Supporting Information for this article is available online:
- Supporting Information
- 1
Lu J.Toy PH. Chem. Rev. 2009, 109: 815 - 2
Hodges JC.Harikrishnan LS.Ault-Justus S. J. Comb. Chem. 2000, 2: 80 -
3a
Lindsley CW.Hodges JC.Filzen GF.Watson BM.Geyer AG. J. Comb. Chem. 2000, 2: 550 -
3b
McAlpine SR.Lindsley CW.Hodges JC.Leonard DM.Filzen GF. J. Comb. Chem. 2001, 3: 1 -
3c
Wisnoski DD.Leister WH.Strauss KA.Zhao Z.Lindsley CW. Tetrahedron Lett. 2003, 44: 4321 -
3d
Fournier D.Pascual S.Montembault V.Haddleton DM.Fontaine L. J. Comb. Chem. 2006, 8: 522 -
3e
Fournier D.Pascual S.Montembault V.Fontaine L. J. Polym. Sci., Part A: Polym. Chem. 2006, 44: 5316 -
3f
Pawluczyk JM.McClain RT.Denicola C.Mulhearn JJ.Rudd DJ.Lindsley CW. Tetrahedron Lett. 2007, 48: 1497 -
3g
Chen G.Tao L.Mantovani G.Geng J.Nystroem D.Haddleton DM. Macromolecules 2007, 40: 7513 - 4
Leung PS.-W.Teng Y.Toy PH. Synlett 2010, 1997 - 5
Leung PS.-W.Teng Y.Toy PH. Org. Lett. 2010, 12: 4996 - For our work regarding cross-linked polymers, see:
-
7a
Kwok M.Choi W.He HS.Toy PH. J. Org. Chem. 2003, 68: 9831 -
7b
Zhao LJ.He HS.Shi M.Toy PH. J. Comb. Chem. 2004, 6: 680 -
7c
Zhao L.-J.Kwong CK.-W.Shi M.Toy PH. Tetrahedron 2005, 61: 12026 - For our work regarding noncross-linked polymers, see:
-
8a
Harned AM.He HS.Toy PH.Flynn DL.Hanson PR. J. Am. Chem. Soc. 2005, 127: 52 -
8b
He HS.Yan JJ.Shen R.Zhuo S.Toy PH. Synlett 2006, 563 -
8c
Kwong CK.-W.Fu MY.Law HC.-H.Toy PH. Synlett 2010, 2617 - 9
Chung CWY.Toy PH. J. Comb. Chem. 2007, 9: 155 - 10
Kwong CK.-W.Huang R.Zhang M.Shi M.Toy PH. Chem. Eur. J. 2007, 13: 2369 - For selected reviews regarding the addition of carbon dioxide to epoxides to form cyclic carbonates, see:
-
11a
Dai W.-L.Luo S.-L.Yin S.-F.Au C.-T. Appl. Catal., A 2009, 366: 2 -
11b
Sakakura T.Kohno K. Chem. Commun. 2009, 1312 -
11c
North M.Pasquale R.Young C. Green Chem. 2010, 12: 1514 - For the organocatalytic addition of carbon dioxide to epoxides, see:
-
12a
Shiels RA.Jones CW. J. Mol. Catal. A: Chem. 2007, 261: 160 ; and references cited therein -
12b
Qi C.Jiang H.Wang Z.Zou B.Yang S. Synlett 2007, 255 -
12c
Barkakaty B.Morino K.Sudo A.Endo T. Green Chem. 2010, 12: 42 - For selected reviews regarding polymer-supported organocatalysts, see:
-
13a
Benaglia M.Puglisi A.Cozzi F. Chem. Rev. 2003, 103: 3401 -
13b
Benaglia M. New J. Chem. 2006, 30: 1525 -
13c
Cozzi F. Adv. Synth. Catal. 2006, 348: 1367 -
13d
Gruttadauria M.Giacalone F.Noto R. Chem. Soc. Rev. 2008, 37: 1666 -
13e
Kristensen TE.Hansen T. Eur. J. Org. Chem. 2010, 3179 - For the use of polymer-supported organocatalysts in the addition of carbon dioxide to epoxides, see:
-
14a
Xie H.Duan H.Li S.Zhang S. New J. Chem. 2005, 29: 1199 -
14b
Du Y.Wang J.-Q.Chen J.-Y.Cai F.Tian J.-S.Kong D.-L.He L.-N. Tetrahedron Lett. 2006, 47: 1271 -
14c
Jagtap SR.Raje VP.Samant SD.Bhanage BM. J. Mol. Catal. A: Chem. 2007, 266: 69 -
14d
Qi C.-R.Jiang H.-F.Wang Z.-Y.Zou B. Chin. J. Chem. 2007, 25: 1051 -
14e
Qi C.Ye J.Zeng W.Jiang H. Adv. Synth. Catal. 2010, 352: 1925 - For the use of other polymers, such as ion-exchange resins, polyaniline salts, and immobilized ionic liquids, to catalyze the addition of carbon dioxide to epoxides, see:
-
15a
Du Y.Cai F.Kong D.-L.He L.-N. Green Chem. 2005, 7: 518 -
15b
He J.Wu T.Zhang Z.Ding K.Han B.Xie Y.Jiang T.Liu Z. Chem. Eur. J. 2007, 13: 6992 -
15c
Xie Y.Zhang Z.Jiang T.He J.Han B.Wu T.Ding K. Angew. Chem. Int. Ed. 2007, 46: 7255 -
16a
Toy PH.Janda KD. Tetrahedron Lett. 1999, 40: 6329 -
16b
Toy PH.Reger TS.Janda KD. Aldrichimica Acta 2000, 33: 87 -
16c
Toy PH.Reger TS.Garibay P.Garno JC.Malikayil JA.Liu G.-Y.Janda KD.
J. Comb. Chem. 2001, 3: 117 -
16d
Choi MKW.Toy PH. Tetrahedron 2004, 60: 2903 - 19
Yue Y.Yu X.-Q.Pu L. Chem. Eur. J. 2009, 15: 5104 -
20a
Bollini M.González M.Bruno AM. Tetrahedron Lett. 2009, 50: 1507 -
20b
Ko K.Nakano K.Watanabe S.Ichikawa Y.Kotsuki H. Tetrahedron Lett. 2009, 50: 4025 -
20c
Deb I.Shanbhag P.Mobin SM.Namboothiri INN. Eur. J. Org. Chem. 2009, 4091 -
20d
Mhasni O.Rezgui F. Tetrahedron Lett. 2010, 51: 586 -
20e
Naidu KC.Babu GR.Gangaiah L.Mukkanti K.Madhusudhan G. Tetrahedron Lett. 2010, 51: 1226 -
20f
Angelini T.Fringuelli F.Lanari D.Pizzo F.Vaccaro L. Tetrahedron Lett. 2010, 51: 1566 -
20g
Goncalves S.Nicolas M.Wagner A.Baati R. Tetrahedron Lett. 2010, 51: 2348 -
20h
Aoki S.Kotani S.Sugiura M.Nakajima M. Tetrahedron Lett. 2010, 51: 3547 -
20i
Hudhomme P. Synlett 2010, 1331 -
20j
Vuluga D.Legros J.Crousse B.Bonnet-Delpon D. Chem. Eur. J. 2010, 16: 1776 -
20k
Helou M.Miserque O.Brusson J.-M.Carpentier J.-F.Guillaume SM. Chem. Eur. J. 2010, 16: 13805
References and Notes
Teng, Y.; Toy, P. H. Synlett 2011, 551.
17See Supporting Information for details.
18
General Procedure
for CO
2
Addition
Reactions
Epoxide 7a-j (22.4 mmol), CH2Cl2 (0.5
mmol), and 4 (0.224 mmol) were placed in
a 25 mL stainless-steel autoclave. Carbon dioxide was then introduced
into the reactor at an initial pressure of 20 bar at r.t. The reactor
was then heated to 120 ˚C, and the pressure was
adjusted to 30 bar. The reaction mixture was stirred under these
conditions for the indicated time, and then the autoclave was cooled
using an ice bath. After releasing the pressure, compound 4 was filtered off and washed with CH2Cl2.
The filtrate was concentrated in vacuo to afford the product 8a-j.
The identity of the products was confirmed by ¹H
NMR.