Ortho-alkylation of o-, m-, and p-cresols with cyclohexene in the presence of aluminum cresolates
We investigated the ortho-alkylation of o-, m-, and p-cresols with cyclohexene in the presence of the corresponding aluminum cresolates in the range of 170-220/sup 0/C in an autoclave in an atmosphere of nitrogen at pressures of 1.0-1.5 MPa. The molar ratios of the cresolates, cyclohexene, and catalysts were varied in the ranges of 301:1-4:0.1-0.3, and the length of the experiment was varied in the range of 2-12 h. The highest selectivity is obtained during the alkylation of p-cresol. The reaction of o-, m-, and p-cresols with cyclohexene in the presence of the corresponding aluminium cresolates leads to mixtures of ethers and phenols, in which the ortho-alkylation products, formed with yields of 75-85%, predominate.
- OSTI ID:
- 6420714
- Journal Information:
- J. Org. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Org. Chem. USSR (Engl. Transl.); (United States) Vol. 23:9; ISSN JOCYA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
400201* -- Chemical & Physicochemical Properties
ALKENES
ALKYLATING AGENTS
ALKYLATION
ALUMINIUM COMPOUNDS
AROMATICS
CATALYTIC EFFECTS
CHEMICAL REACTIONS
CHROMATOGRAPHY
CRESOLS
CYCLOALKENES
ETHERS
HYDROCARBONS
HYDROXY COMPOUNDS
INFRARED SPECTRA
NMR SPECTRA
ORGANIC COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
PHENOLATES
PHENOLS
SEPARATION PROCESSES
SPECTRA
STRUCTURAL CHEMICAL ANALYSIS