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4-tert-Butyl-1-(1-naphth­yl)cyclo­hexene

✍ Scribed by Periasamy, M. ;Soundirapandian, Sudha ;Athimoolam, S. ;Ponnusamy, A. ;Natarajan, S.


Publisher
International Union of Crystallography
Year
2006
Tongue
English
Weight
281 KB
Volume
62
Category
Article
ISSN
1600-5368

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✦ Synopsis


In the title compound, C 20 H 24 , the central cyclohexene ring is in a distorted half-chair conformation. The crystal structure is stabilized by weak van der Waals interactions.


📜 SIMILAR VOLUMES


1-(4-tert-Butyl­phen­yl)-3-hydr­oxy-3-(2
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The crystal structure of the title compound, C 23 H 22 O 2 , which exists in the enol form, is stabilized by an intramolecular hydrogen bond. The dihedral angle between the naphthyl ring system and the aromatic ring of the t-BuC 6 H 4 group is 23.50 (10) .

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The title compound, C 20 H 21 NO, was obtained by the reaction of indole-3-carbaldehyde with 4-tert-butylbenzyl chloride and recrystallization of the product from ethanol. The indole ring system is nearly planar and makes a dihedral angle of 74.45 (3) with the plane of the 4-tert-butylphenyl ring.