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DOI: 10.1055/s-0030-1259029
Organic Reactions in Water: A Practical and Convenient Method for the N-Formylation of Amines in Water
Publication History
Publication Date:
10 November 2010 (online)

Abstract
A simple, efficient, scaleable process has been developed for the N-formylation amines in water. Treatment of amines with triethyl orthoformate in water at reflux under neutral conditions without any additives gives the corresponding N-formyl derivatives in good yields.
Key words
N-formylation - amines - organic reactions in water - triethyl orthoformate
- 1
Jackson A.Meth-Cohn O. J. Chem. Soc., Chem. Commun. 1995, 1319 - 2
Chen B.-C.Bednarz MS.Zhao R.Sundeen JE.Chen P.Shen Z.Skoumbourdis AP.Barrish JC. Tetrahedron Lett. 2000, 41: 5453 - 3a
Kobayashi K.Nagato S.Kawakita M.Morikawa O.Konishi H. Chem. Lett. 1995, 575MissingFormLabel - 3b
Kakehi A.Ito S.Hayashi S.Fujii T. Bull. Chem. Soc. Jpn. 1995, 68: 3573MissingFormLabel - 4
Han Y.Cai L. Tetrahedron Lett. 1997, 38: 5423 - 5
Mahmoud KF, andNewtown SP. inventors; US 5,155,267.MissingFormLabel - 6
Dieter A, andGerhard K. inventors; US 4,419,297.MissingFormLabel - 7
Downie IM.Earle MJ.Heaney H.Shuhaibar KF. Tetrahedron 1993, 49: 4015 - 8a
Kobayashi S.Nishio K. J. Org. Chem. 1994, 59: 6620MissingFormLabel - 8b
Clayden J. Organic Chemistry Oxford University Press; Oxford: 2001. p.276-296MissingFormLabel - 8c
Kobayashi S.Yasuda M.Hachiya I. Chem. Lett. 1996, 407MissingFormLabel - 9a
Green TW.Wuts PGM. Protective Groups in Organic Synthesis 3rd ed.: Wiley-Interscience; New York: 1999.MissingFormLabel - 9b
Sheehan JC.Yang DDH. J. Am. Chem. Soc. 1958, 80: 1154MissingFormLabel - 9c
Strazzolini P.Giumanini AG.Cauci S. Tetrahedron 1990, 46: 1081MissingFormLabel - 9d
Blicke FF.Lu C.-J.
J. Am. Chem. Soc. 1952, 74: 3933MissingFormLabel - 9e
Waki J.Meienhofer J. J. Org. Chem. 1977, 42: 2019MissingFormLabel - 9f
Chen FMF.Benoiton NL. Synthesis 1979, 709MissingFormLabel - 9g
Yale HL. J. Org. Chem. 1971, 36: 3238MissingFormLabel - 9h
Kisfaludy L.Laszlo O. Synthesis 1987, 510MissingFormLabel - 9i
Neveux M.Bruneaum C.Dixneuf PH. J. Chem. Soc., Perkin Trans. 1 1991, 1197MissingFormLabel - 10
Duezek W.Deutsch J.Vieth S.Nicolas H.-J. Synthesis 1996, 37 - 11
Mihara M.Ishino Y.Minakata S.Komatsu M. Synthesis 2003, 2317 - 12
Reddy PG.Kumar GDK.Baskaran S. Tetrahedron 2000, 41: 9149 - 13
Luca LD.Giacomelli G.Porcheddu A.Salaris M. Synlett 2004, 2570 - 14
Desai B.Danks TN.Wagner G. Tetrahedron Lett. 2005, 46: 955 - 15a
Hosseini-Sarvari M.Sharghi J. J. Org. Chem. 2006, 71: 6652MissingFormLabel - 15b
Khazaei A.Mehdipour E. Iran Polym. J. 1999, 8: 257MissingFormLabel - 15c
Bao K.Zhang W.Bu X.Song Z.Zhang L.Cheng M. Chem. Commun. 2008, 5428MissingFormLabel - 15d
Tumma H.Nagaraju N.Reddy KV. J. Mol. Catal. A: Chem. 2009, 310: 121MissingFormLabel - 15e
Brahmachari G.Laskar S. Tetrahedron Lett. 2010, 51: 2319MissingFormLabel - 16
Ishida T.Haruta M. Chem. Commun. 2009, 538 - 17a
Chancellor T.Morton C. Synthesis 1994, 1023MissingFormLabel - 17b
Roberts R.Vogt P. J. Am. Chem. Soc. 1956, 78: 4778MissingFormLabel - 17c
Swaringen R.Eaddy J.Henderson T. J. Org. Chem. 1980, 45: 3986MissingFormLabel - 18a
Grieco PA. Organic Synthesis in Water Blackie Academic and Professional; London: 1998.MissingFormLabel - 18b
Demko ZP.Sharpless KB. J. Org. Chem. 2001, 66: 7945MissingFormLabel - 18c
Li C.-J. Chem. Rev. 2005, 105: 3095MissingFormLabel - 18d
Azizi N.Aryanasab F.Torkiyan L.Ziyaei A.Saidi MR. J. Org. Chem. 2006, 71: 3634MissingFormLabel - 18e
Kaboudin B.Sorbiun M. Tetrahedron Lett. 2007, 48: 9015MissingFormLabel - 19a
Balakrishna MS.Kaboudin B. Tetrahedron Lett. 2001, 42: 1127MissingFormLabel - 19b
Kaboudin B.Navaee K. Heterocycles 2001, 55: 1443MissingFormLabel - 19c
Kaboudin B.Navaee K. Heterocycles 2003, 60: 2287MissingFormLabel - 19d
Kaboudin B.Saadati F. J. Heterocycl. Chem. 2005, 42: 699MissingFormLabel - 19e
Kaboudin B.Saadati F. Heterocycles 2005, 65: 353MissingFormLabel - 19f
Kaboudin B.Rahmani A. Synthesis 2003, 2705MissingFormLabel - 19g
Kaboudin B.Saadati F. Synthesis 2004, 1249MissingFormLabel - 19h
Kaboudin B.Rahmani A. Org. Prep. Proced. Int. 2004, 36: 82MissingFormLabel - 19i
Kaboudin B.Moradi K. Tetrahedron Lett. 2005, 46: 2989MissingFormLabel - 19j
Kaboudin B.Haghighat H. Tetrahedron Lett. 2005, 46: 7955MissingFormLabel - 19k
Kaboudin B.Haghighat H.Yokomatsu T. J. Org. Chem. 2006, 71: 6604MissingFormLabel - 19l
Kaboudin B.Karimi M. Bioorg. Med. Chem. Lett. 2006, 16: 5324MissingFormLabel - 19m
Kaboudin B.Farjadian F. Beilstein J. Org. Chem. 2006, 2: 4MissingFormLabel - 19n
Yamagishi T.Kusano T.Kaboudin B.Yokomatsu T.Sakuma C.Shibuya S. Tetrahedron 2003, 59: 767MissingFormLabel - 19o
Kaboudin B.Haruki T.Yamaghishi T.Yokomatsu T. Tetrahedron 2007, 63: 8199MissingFormLabel - 19p
Kaboudin B.Haruki T.Yamagishi T.Yokomatsu T. Synthesis 2007, 3226MissingFormLabel - 19q
Kaboudin B.Haghighat H.Yokomatsu T. Tetrahedron: Asymmetry 2008, 19: 862MissingFormLabel - 19r
Kaboudin B.Saadati F. Tetrahedron Lett. 2009, 50: 1450MissingFormLabel
References and Notes
The amine (3 mmol) and triethyl orthoformate
(12 mmol) was added to H2O (8 mL), and the solution was
stirred for 3-48 h at reflux or 2-3 h under microwave
irradiation at 90 ˚C at ambient pressure in a
microwave reactor (a Milestone, Micro SYNTH Microwave Labstation
for Synthesis, microwave reactor was used for all experiments).
After stirring for the requisite period (Table
[¹]
), the reaction mixture
was washed with Et2O (3 × 50
mL). The resulting mixture was subjected to column chromatography
on silica gel with EtOAc-n-hexane
(2:8) and evaporation of the solvent under reduced pressure to give
pure products in
41-87% yields. All
products gave satisfactory spectroscopic data according to the literature.¹5