Hydrocarbons and alcohols of Chamesyce canescens

Chemistry of Natural Compounds, May 1971

A. I. Nuritdinova, Z. N. Nazirov, A. K. Karimdzhanov

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Hydrocarbons and alcohols of Chamesyce canescens

BRIEF COMMUNICATIONS HYDROCARBONS AND ALCOHOLS OF Chamesyce eaneseens A. I . N u r i t d i n o v a , Z . N. N a z i r o v , and A. K. Karimdzhanov UDC 547.219.16 We have investigated the epigeal p a r t of C h a m e s y c e c a n e s c e n s , family Euphorbiaceae, collected in full-flowering period in the Tashkent oblast. The e o m m i n u t e d plant m a t e r i a l was e x t r a c t e d with c h l o r o f o r m . The yield of e x t r a c t i v e s u b s t a n c e s was 5.99%, of which the a c e t o n e - s o l u b l e f r a c t i o n amounted to 4.46% and the insoluble fraction to 1.53%. The a c e t o n e - i n s o l u b l e f r a c t i o n was heated with p e t r o l e u m e t h e r (bp 40-70°C). The fraction soluble in p e t roleum e t h e r was p a s s e d through a column filled with alumina (length of the column 70 cm, d i a m e t e r 3.4 cm). The column was eluted s u c c e s s i v e l y with p e t r o l e u m ether, benzene, diethyl ether, acetone, and m e t h anol. The f i r s t f r a c t i o n (petroleum ether) yielded the h y d r o c a r b o n dotriacontane, C32H66, m p 69-70°C [1, 2]; the benzene f r a c t i o n yielded the h y d r o c a r b o n triacontane, C30H62, with mp 65-66°C [2, 3]; and the subsequent f r a c t i o n s ( d i e t h y l e t h e r ) y i e l d e d dotriacontanol, C32H6~OH, with mp 87-88°C [1], and triacontanol, C30H61OH, with mp 85-86°C [2, 3]. T h e s e s u b s t a n c e s w e r e identified with authentic s a m p l e s by m i x e d melting points, e l e m e n t a r y a n a l y s i s , and IR s p e c t r a . This is the f i r s t t i m e that the h y d r o c a r b o n s and alcohols mentioned have been isolated f r o m the genus Chamesyce. LITERATURE 1. 2. 3. CITED A. S. Sadykov, Kh. I. Isaev, and A. I. I s m a i l o v , Uzb. Khim. Zh., 1963, No. 2, 53. U. Kh. Khalimova, I. Kadyrov, Kh. I s a e v , and A. I s m a i l o v , Khim. Prirodn. Soedin., 6, 756 (1970). G. Jenkins and W. Hartung, The C h e m i s t r y of Organic Medicinal Products, 2nd ed., John Wiley, New Y o r k (1943). Tashkent P h a r m a c e u t i c a l Institute. T r a n s l a t e d f r o m Khimiya Prirodnykh Soedinenii, No. 3, pp. 367368, M a y - J u n e , 1971. Original a r t i c l e submitted F e b r u a r y 15, 1971. © 1973 Consultants Bureau, a division of Plenum Publishing Corporation, 227 West 17th Street, New York, N. Y. 10011. All rights reserved. This article cannot be reproduced for any purpose whatsoever without permission of the publisher. A copy of this article is available from the publisher for $15.00. 342 (...truncated)


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A. I. Nuritdinova, Z. N. Nazirov, A. K. Karimdzhanov. Hydrocarbons and alcohols of Chamesyce canescens, Chemistry of Natural Compounds, 1971, pp. 342-342, Volume 7, Issue 3, DOI: 10.1007/BF00569010