Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 2004(9): 1575-1576
DOI: 10.1055/s-2004-829535
DOI: 10.1055/s-2004-829535
LETTER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Aromatic Aldehydes by Oxidative Hydroxymethylation
Further Information
Received
1 April 2004
Publication Date:
29 June 2004 (online)
Publication History
Publication Date:
29 June 2004 (online)
Abstract
A new high yield method for the synthesis of aromatic aldehydes has been developed. The procedure is based on an acid catalyzed hydroxymethylation of an arene substrate by paraformaldehyde with concurrent selective oxidation of the intermediate aromatic carbinol by 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) to the aldehyde product.
Key words
aldehydes - arenes - electrophilic aromatic substitutions - oxidations - quinones
- 1
Haines AH. Methods for the Oxidation of Organic Compounds Academic Press; London: 1988. - 2
Rylander PN. Catalytic Hydrogenation in Organic Syntheses Academic Press; New York: 1979. - 3
Heck RF. Palladium Reagents in Organic Syntheses Academic Press; London: 1985. - 4
Crounse NN. Org. React. 1949, 5: 290 - 5
Truce WE. Org. React. 1957, 9: 37 - 6
Jutz C. Adv. Org. Chem. 1976, 9: 225 - 7
Wynberg H.Meijer EW. Org. React. 1982, 28: 1 - 8
Reiche A.Gross H.Höft E. Chem. Ber. 1960, 93: 88 - 9
Olah GA.Kuhn SJ. J. Am. Chem. Soc. 1960, 82: 2380 -
10a
Casnati G,Casiraghi G,Puglia G,Sartori G, andTerenghi G. inventors; US Patent 4,151,201. -
10b
Casiraghi G.Casnati G.Puglia G.Sartori MG.Terenghi G. J. Chem. Soc., Perkin Trans. 1 1980, 1862 -
10c
Furukawa Y, andKeishi K. inventors; US Patent 6,080,895. - 11
Matsuda T, andMurata T. inventors; US Patent 4,231,967. - 12
Lee RJ, andBaranowski LJ. inventors; US Patent 4,371,712. - 13
Virnig MJ. inventors; US Patent 4,638,096. - 14
Bigi F.Conforti ML.Maggi R.Sartori G. Tetrahedron 2000, 56: 2709 - 15
Jyothi TM.Talawar MB.Rao BS. Catal. Lett. 2000, 64: 151 -
16a
Becker HD.Bjoerk A.Adler E. J. Org. Chem. 1980, 45: 1596 -
16b
Khenkin AM.Vigdergauz I.Neumann R. Chem.-Eur. J. 2000, 6: 875 ; and references therein -
17a
Newman MS.Khanna VK. Org. Prep. Proced. Int. 1985, 17: 422 -
17b
Kim KH.Grunewald GL. Org. Prep. Proced. Int. 1976, 8: 141