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Abstract

The apparatus used in the preparation of furan is shown in Fig. 2. The round-bottomed flask A has a side neck which carries a thermometer B reaching almost to the bottom of the flask. The mouth of the flask is closed with a rubber bung through which passes the vertical tube C, 15 cm in length and 1.8–2.0 cm in diameter. The upper end of the tube C is closed with a rubber stopper, which carries a long glass rod D; this is used for pushing sublimed 2-furoic acid back into the flask. A side tube E, diameter 1.8–2.0 cm, is fused to the vertical tube C at 2.5–3 cm from its upper end. The narrower (diameter 1 cm) vertical part of the tube E ends at the bottom of the column F, which is 3.5–4 cm in diameter and 25 cm in height. The column F is filled with pieces of sodium hydroxide of the size of a pea, which are separated from the end of the tube E by a layer of cotton wool (Note 1). The column F is immersed in a water bath (a tall beaker) at 45–50°. The exit tube of the column F is connected to a sloping condenser attached to a receiver immersed in ice and salt (Note 2).

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Literature Cited

  1. C. D. Hurd, A. R. Goldsby, and E. N. Osborne, J. Am. Chem. Soc. 54, 2532 (1932).

    Article  CAS  Google Scholar 

  2. V. A. Kozin, Zh. priklad. khim. (J. Appl. Chem.) 26, 442 (1953).

    Google Scholar 

  3. O. W. Cass, Ind. Eng. Chem. 40, 216 (1948).

    Article  CAS  Google Scholar 

  4. U. S. Pat. 2,634,276 (1953);

    Google Scholar 

  5. C. A. 48, 2115b (1954).

    Google Scholar 

  6. Italian Pat. 421,626 (1947);

    Google Scholar 

  7. C. A. 43, 5047g (1949).

    Google Scholar 

  8. H. E. Eschinazi, Bull. soc. chim. 967 (1952).

    Google Scholar 

  9. P. Freundler, C.r. 124, 1157 (1897);

    Google Scholar 

  10. Bull, soc. chim. (3) 17, 613 (1897). R H. Limpricht, A. 165, 281 (1878).

    Google Scholar 

  11. E. C. Wagner and J. K. Simons, J. Chem. Educ. 13, 270 (1936);

    Google Scholar 

  12. H. Narasaki and N. Ito, Repts. Govt. Chem. Ind. Research Inst. Tokyo 46, 199 (1951);

    Google Scholar 

  13. C. A. 46, 4524b (1952).

    Google Scholar 

  14. Organic Syntheses (Russian Translation), Vol. 1, P. 449, Foreign Lit. Press, Moscow, 1949 [Organic Syntheses, Collective Vol. 1, 2nd Ed., New York and London, 1941, p. 274.]

    Google Scholar 

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Authors

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A. L. Mndzhoian

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© 1959 Springer Science+Business Media New York

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Mndzhoian, A.L. (1959). Furan. In: Mndzhoian, A.L. (eds) Syntheses of Heterocyclic Compounds. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-6658-5_19

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  • DOI: https://doi.org/10.1007/978-1-4757-6658-5_19

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-6660-8

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