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
References and Notes
<A NAME="RD15910ST-1">1 </A>
Jackson A.
Meth-Cohn O.
J. Chem. Soc., Chem. Commun.
1995,
1319
<A NAME="RD15910ST-2">2 </A>
Chen B.-C.
Bednarz MS.
Zhao R.
Sundeen JE.
Chen P.
Shen Z.
Skoumbourdis AP.
Barrish JC.
Tetrahedron Lett.
2000,
41:
5453
<A NAME="RD15910ST-3A">3a </A>
Kobayashi K.
Nagato S.
Kawakita M.
Morikawa O.
Konishi H.
Chem. Lett.
1995,
575
<A NAME="RD15910ST-3B">3b </A>
Kakehi A.
Ito S.
Hayashi S.
Fujii T.
Bull. Chem. Soc. Jpn.
1995,
68:
3573
<A NAME="RD15910ST-4">4 </A>
Han Y.
Cai L.
Tetrahedron Lett.
1997,
38:
5423
<A NAME="RD15910ST-5">5 </A>
Mahmoud KF, and
Newtown SP. inventors; US 5,155,267.
<A NAME="RD15910ST-6">6 </A>
Dieter A, and
Gerhard K. inventors; US 4,419,297.
<A NAME="RD15910ST-7">7 </A>
Downie IM.
Earle MJ.
Heaney H.
Shuhaibar KF.
Tetrahedron
1993,
49:
4015
<A NAME="RD15910ST-8A">8a </A>
Kobayashi S.
Nishio K.
J.
Org. Chem.
1994,
59:
6620
<A NAME="RD15910ST-8B">8b </A>
Clayden J.
Organic Chemistry
Oxford
University Press;
Oxford:
2001.
p.276-296
<A NAME="RD15910ST-8C">8c </A>
Kobayashi S.
Yasuda M.
Hachiya I.
Chem.
Lett.
1996,
407
<A NAME="RD15910ST-9A">9a </A>
Green TW.
Wuts PGM.
Protective Groups in Organic
Synthesis
3rd ed.:
Wiley-Interscience;
New
York:
1999.
<A NAME="RD15910ST-9B">9b </A>
Sheehan JC.
Yang DDH.
J.
Am. Chem. Soc.
1958,
80:
1154
<A NAME="RD15910ST-9C">9c </A>
Strazzolini P.
Giumanini AG.
Cauci S.
Tetrahedron
1990,
46:
1081
<A NAME="RD15910ST-9D">9d </A>
Blicke FF.
Lu C.-J.
J.
Am. Chem. Soc.
1952,
74:
3933
<A NAME="RD15910ST-9E">9e </A>
Waki J.
Meienhofer J.
J. Org. Chem.
1977,
42:
2019
<A NAME="RD15910ST-9F">9f </A>
Chen FMF.
Benoiton NL.
Synthesis
1979,
709
<A NAME="RD15910ST-9G">9g </A>
Yale HL.
J. Org. Chem.
1971,
36:
3238
<A NAME="RD15910ST-9H">9h </A>
Kisfaludy L.
Laszlo O.
Synthesis
1987,
510
<A NAME="RD15910ST-9I">9i </A>
Neveux M.
Bruneaum C.
Dixneuf PH.
J.
Chem. Soc., Perkin Trans. 1
1991,
1197
<A NAME="RD15910ST-10">10 </A>
Duezek W.
Deutsch J.
Vieth S.
Nicolas H.-J.
Synthesis
1996,
37
<A NAME="RD15910ST-11">11 </A>
Mihara M.
Ishino Y.
Minakata S.
Komatsu M.
Synthesis
2003,
2317
<A NAME="RD15910ST-12">12 </A>
Reddy PG.
Kumar GDK.
Baskaran S.
Tetrahedron
2000,
41:
9149
<A NAME="RD15910ST-13">13 </A>
Luca LD.
Giacomelli G.
Porcheddu A.
Salaris M.
Synlett
2004,
2570
<A NAME="RD15910ST-14">14 </A>
Desai B.
Danks TN.
Wagner G.
Tetrahedron
Lett.
2005,
46:
955
<A NAME="RD15910ST-15A">15a </A>
Hosseini-Sarvari M.
Sharghi J.
J.
Org. Chem.
2006,
71:
6652
<A NAME="RD15910ST-15B">15b </A>
Khazaei A.
Mehdipour E.
Iran Polym. J.
1999,
8:
257
<A NAME="RD15910ST-15C">15c </A>
Bao K.
Zhang W.
Bu X.
Song Z.
Zhang L.
Cheng M.
Chem.
Commun.
2008,
5428
<A NAME="RD15910ST-15D">15d </A>
Tumma H.
Nagaraju N.
Reddy KV.
J.
Mol. Catal. A: Chem.
2009,
310:
121
<A NAME="RD15910ST-15E">15e </A>
Brahmachari G.
Laskar S.
Tetrahedron Lett.
2010,
51:
2319
<A NAME="RD15910ST-16">16 </A>
Ishida T.
Haruta M.
Chem. Commun.
2009,
538
<A NAME="RD15910ST-17A">17a </A>
Chancellor T.
Morton C.
Synthesis
1994,
1023
<A NAME="RD15910ST-17B">17b </A>
Roberts R.
Vogt P.
J. Am. Chem. Soc.
1956,
78:
4778
<A NAME="RD15910ST-17C">17c </A>
Swaringen R.
Eaddy J.
Henderson T.
J.
Org. Chem.
1980,
45:
3986
<A NAME="RD15910ST-18A">18a </A>
Grieco PA.
Organic
Synthesis in Water
Blackie Academic and Professional;
London:
1998.
<A NAME="RD15910ST-18B">18b </A>
Demko
ZP.
Sharpless KB.
J.
Org. Chem.
2001,
66:
7945
<A NAME="RD15910ST-18C">18c </A>
Li C.-J.
Chem.
Rev.
2005,
105:
3095
<A NAME="RD15910ST-18D">18d </A>
Azizi N.
Aryanasab F.
Torkiyan L.
Ziyaei A.
Saidi MR.
J.
Org. Chem.
2006,
71:
3634
<A NAME="RD15910ST-18E">18e </A>
Kaboudin B.
Sorbiun M.
Tetrahedron Lett.
2007,
48:
9015
<A NAME="RD15910ST-19A">19a </A>
Balakrishna MS.
Kaboudin B.
Tetrahedron
Lett.
2001,
42:
1127
<A NAME="RD15910ST-19B">19b </A>
Kaboudin B.
Navaee K.
Heterocycles
2001,
55:
1443
<A NAME="RD15910ST-19C">19c </A>
Kaboudin B.
Navaee K.
Heterocycles
2003,
60:
2287
<A NAME="RD15910ST-19D">19d </A>
Kaboudin B.
Saadati F.
J. Heterocycl. Chem.
2005,
42:
699
<A NAME="RD15910ST-19E">19e </A>
Kaboudin B.
Saadati F.
Heterocycles
2005,
65:
353
<A NAME="RD15910ST-19F">19f </A>
Kaboudin B.
Rahmani A.
Synthesis
2003,
2705
<A NAME="RD15910ST-19G">19g </A>
Kaboudin B.
Saadati F.
Synthesis
2004,
1249
<A NAME="RD15910ST-19H">19h </A>
Kaboudin B.
Rahmani A.
Org. Prep. Proced. Int.
2004,
36:
82
<A NAME="RD15910ST-19I">19i </A>
Kaboudin B.
Moradi K.
Tetrahedron Lett.
2005,
46:
2989
<A NAME="RD15910ST-19J">19j </A>
Kaboudin B.
Haghighat H.
Tetrahedron Lett.
2005,
46:
7955
<A NAME="RD15910ST-19K">19k </A>
Kaboudin B.
Haghighat H.
Yokomatsu T.
J.
Org. Chem.
2006,
71:
6604
<A NAME="RD15910ST-19L">19l </A>
Kaboudin B.
Karimi M.
Bioorg. Med. Chem. Lett.
2006,
16:
5324
<A NAME="RD15910ST-19M">19m </A>
Kaboudin B.
Farjadian F.
Beilstein J. Org. Chem.
2006,
2:
4
<A NAME="RD15910ST-19N">19n </A>
Yamagishi T.
Kusano T.
Kaboudin B.
Yokomatsu T.
Sakuma C.
Shibuya S.
Tetrahedron
2003,
59:
767
<A NAME="RD15910ST-19O">19o </A>
Kaboudin B.
Haruki T.
Yamaghishi T.
Yokomatsu T.
Tetrahedron
2007,
63:
8199
<A NAME="RD15910ST-19P">19p </A>
Kaboudin B.
Haruki T.
Yamagishi T.
Yokomatsu T.
Synthesis
2007,
3226
<A NAME="RD15910ST-19Q">19q </A>
Kaboudin B.
Haghighat H.
Yokomatsu T.
Tetrahedron:
Asymmetry
2008,
19:
862
<A NAME="RD15910ST-19R">19r </A>
Kaboudin B.
Saadati F.
Tetrahedron Lett.
2009,
50:
1450
<A NAME="RD15910ST-20">20 </A>
The amine (3 mmol) and triethyl orthoformate
(12 mmol) was added to H2 O (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 Et2 O (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