کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1325267 1499945 2009 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Activation of C–H bonds of hydrocarbons by the ArH–alkali metal systems in THF (ArH – naphthalene, biphenyl, anthracene, phenanthrene, trans-stilbene, pyrene). Alkylation of naphthalene and toluene with ethene
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Activation of C–H bonds of hydrocarbons by the ArH–alkali metal systems in THF (ArH – naphthalene, biphenyl, anthracene, phenanthrene, trans-stilbene, pyrene). Alkylation of naphthalene and toluene with ethene
چکیده انگلیسی

Systems based on naphthalene and alkali metals (Li, Na, K) in THF are able to induce the alkylation of naphthalene with ethene at room temperature and atmospheric pressure. The highest activity in this reaction is exhibited by the naphthalene–potassium system which converts naphthalene into 1-ethylnaphthalene (1) and small amounts of two isomeric dihydro derivatives of 1 in a yield of 85% (24 h, K:C10H8 = 2:1). The same alkylation products are formed when metallic sodium is used instead of potassium. The interaction of ethene with the naphthalene–lithium system (24 h, Li:C10H8 = 2:1) affords 1 together with 1-n-butylnaphthalene (4), 1-n-hexylnaphthalene (5), 1-n-oktylnaphthalene (6) and dihydro derivatives of 5 and 6 in a total yield of 60%. Alkylation of toluene with ethene in the naphthalene–alkali metal systems leads to the formation of higher monoalkylbenzenes. The greatest toluene conversion (48%, 24 h) is observed on using the lithium-containing system (Li:C10H8 = 2:1), in the presence of which a mixture of n-propylbenzene (11), n-pentylbenzene (12), 3-phenylpentane (13) and 3-phenylheptane (14) is produced from ethene and toluene. On the replacement of lithium by sodium or potassium, only 11 and 13 are obtained. A treatment of biphenyl, phenanthrene, trans-stilbene, pyrene and anthracene with alkali metals in THF also gives systems capable of catalyzing the alkylation of toluene with ethene at 22 °C. Of particularly active is the stilbene–lithium system (Li:stilbene = 3:1) which converts toluene into a mixture of 11–14, n-heptylbenzene and 5-phenylnonane in a yield of 58%. In all cases, the rate of the alkylation considerably increases in the presence of the solid phase of alkali metal. The mechanism of the reactions found is discussed.

The paper reports on the remarkable ability of the naphthalene–alkali metal systems in THF to induce the naphthalene and toluene alkylation with ethene at room temperature. Data on alkylation of toluene in the analogous systems based on biphenyl, anthracene, trans-stilbene, phenanthrene and pyrene are also presented.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Organometallic Chemistry - Volume 694, Issues 9–10, 15 April 2009, Pages 1459–1466
نویسندگان
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