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Title: Upgrading of coal liquids by O-alkylation of phenols with olefins. Part 1. Reaction with branched olefins

Conference · · Am. Chem. Soc., Div. Pet. Chem., Prepr.; (United States)
OSTI ID:6612955

The objective is to formulate a process for obtaining high yields of ether products while minimizing the polymerization and carbon alkylation side reactions. 2-methyl-2-butene was chosen as the alkylating agent, and p-cresol is the first model compound. The effect of temperature on the products from 4 h reactions in 40% sulfuric acid was measured. The values reported are those of equilibrium since ether formation is a reversible process. Results indicate that equilibrium in the forward direction is favored at lower temperatures. Reduced temperatures also decrease the amount of ring alkylation. The use of 10% sulfuric acid also reduced ring alkylation, but the rate of ether formation is reduced. Thus, increasing the olefin/phenol ratio can be expected to increase ether formation. 12 figures, 9 tables.

Research Organization:
Exxon Research and Engineering Co., Linden, NJ
OSTI ID:
6612955
Report Number(s):
CONF-820909-Vol.2
Journal Information:
Am. Chem. Soc., Div. Pet. Chem., Prepr.; (United States), Vol. 27:4; Conference: National meeting of the American Chemical Society, Kansas City, MO, USA, 1 Sep 1982
Country of Publication:
United States
Language:
English

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