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Synthesis 2003(12): 1869-1871
DOI: 10.1055/s-2003-41001
DOI: 10.1055/s-2003-41001
SHORTPAPER
© Georg ThiemeVerlag Stuttgart · New York
A Novel and Efficient Synthesisof Camphorquinone from Camphoric Acid
Further Information
Received
21 April 2003
Publication Date:
07 August 2003 (online)
Publication History
Publication Date:
07 August 2003 (online)
Abstract
Camphorquinone (1), an important finechemical and medicinal product derived from camphor, was efficientlysynthesized from easily available camphoric acid (2).The key steps include acyloin condensation using Me3SiClas a scavenger of alkoxides and oxidation of the bis(trimethylsilyl)derivative 4 by bromine in CCl4.The new method offers an efficient alternative synthesis of camphorquinone(1).
Key words
camphor - camphorquinone - cyclization - condensation
- 1
Linden LA. In Radiation Curing in Polymer Science and Technology,IVFouassier J.Rabek JF. Elsevier AppliedScience; London: 1993. p.382-398 - 2
Munksguard EC.Iire M.Asmunssen E. J.Dent. Res. 1986, 64: 1409 - 3
Park YJ.Chae KH.Rawls HR. Dent.Mat. 1999, 15: 120 - 4
Bornner MP.Thornton ER. J. Am. Chem. Soc. 1991, 113: 1299 - 5
Ellis MK.Golding BT.Maude AB.Watson WP. J. Chem.Soc., Perkin. Trans. 1 1991, 747 - 6
Evans WC.Ridgion JM.Simonsen JL. J. Chem. Soc. 1934, 137 - 7
Barton DHR.Hui RAHF.Lester DJ.Ley SV. TetrahedronLett. 1979, 20: 3331 - 8
Hattori K.Yoshida T.Rikuta K.Miyakoshi T. Chem. Lett. 1994, 1885 - 9
Vedejs E.Engler DA.Telschow JE. J. Org. Chem. 1978, 43: 188 - 10
Chaussin R.Leriverend P.Pacquer P. J.Chem. Soc., Chem. Commun. 1978, 1032 - 11
Barton DHR.Cussans NJ.Ley SV. J. Chem. Soc., Chem. Commun. 1978, 393 - 12
Okada K.Mukai T. Tetrahedron Lett. 1980, 21: 359 - 13
Creary X. J.Org. Chem. 1980, 45: 2419 - 14
Burgstahler AW.Boger DL.Naik NC. Tetrahedron 1976, 32: 309 - 15
Herzog H.Scharf HD. Synthesis 1986, 788 - 16
Langlois N.Langlois Y.Chiaroni A.Riche C. Tetrahedron Lett. 1989, 30: 1395 - 17
Hazardsin the Chemical Laboratory
Luxon SG. Royal Society of Chemistry; Cambridge: 1992. 5thed.. p.567 - 18
Manufacture JRB. inventors; French Patent 1511610. ; Chem. Abstr. 1969, 70, 68569 - 19
Aishin O.Yasuzo O.Minoru I. Chem.High Polym. 1950, 7: 365 ; Chem. Abstr. 1953, 47, 3822 -
20a
Bloomfield JJ.Owsley DC.Nelke JM. Org.React. 1976, 23: 259 -
20b
Finley KT. Chem. Rev. 1964, 64: 573 - 21
Rühlmann K. Synthesis 1971, 236 -
22a
Bloomfield JJ. Tetrahedron Lett. 1968, 587 -
22b
Bloomfield JJ. Tetrahderon Lett. 1968, 591 -
23a
Philip B.Jeung HS. Synth.Commun. 1986, 16: 775 -
23b
Hiroshi YN.Prabhakar R.Masato T. Chem. Lett. 1993, 315 -
23c
Rasmussen JK.Krepski LR.Heilmann SM.Smith HKII.Tumey ML. Synthesis 1983, 457 -
23d
Tanaka M, andYamashita H. inventors; Japanese Patent 05202077. ; Chem. Abstr. 1994, 120, 246099 - 24
Fuschler HM.Heine HG.Hartmann W. Tetrahedron Lett. 1972, 860 - 25
Strating J.Reiffers S.Wynberg H. Synthesis 1971, 211