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1,4-Bis(1,1-dimethyl-prop-yl)-2,5-dimeth-oxy-benzene.


ABSTRACT: The title compound, C(18)H(30)O(2), was prepared by Friedel-Crafts alkyl-ation of 1,4-dimeth-oxy-benzene with 2-methyl-2-butanol. The complete mol-ecule is generated by the application of a crystallographic centre of inversion. The two meth-oxy groups are oriented in the same plane of the aromatic ring [C-C-O-C torsion angle = 9.14?(16)°]. While one methyl group of the tert-pentyl substituent is coplanar with the benzene ring [C-C-C-C = 0.45?(15)°] and lies towards the less-hindered H atom, the other methyl and ethyl groups are directed to either side of the benzene ring [C-C-C-C torsion angles = 118.78?(12) and 59.11?(14)°, respectively]. In the crystal, the hydro-phobic mol-ecules pack to form a brick-wall-like architecture.

SUBMITTER: Amimoto K 

PROVIDER: S-EPMC3201239 | biostudies-literature | 2011 Oct

REPOSITORIES: biostudies-literature

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1,4-Bis(1,1-dimethyl-prop-yl)-2,5-dimeth-oxy-benzene.

Amimoto Kiichi K  

Acta crystallographica. Section E, Structure reports online 20110930 Pt 10


The title compound, C(18)H(30)O(2), was prepared by Friedel-Crafts alkyl-ation of 1,4-dimeth-oxy-benzene with 2-methyl-2-butanol. The complete mol-ecule is generated by the application of a crystallographic centre of inversion. The two meth-oxy groups are oriented in the same plane of the aromatic ring [C-C-O-C torsion angle = 9.14 (16)°]. While one methyl group of the tert-pentyl substituent is coplanar with the benzene ring [C-C-C-C = 0.45 (15)°] and lies towards the less-hindered H atom, the  ...[more]

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