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Preparation of o-benzylphenol

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TLDR
In this paper, a process for preparing o-benzylphenol in high selectivity is described, which comprises heating a mixture of benzyl alcohol and phenol in the presence of an effective amount of activated alumina as a catalyst.
Abstract
A process for preparing o-benzylphenol in high selectivity is disclosed. The process comprises heating a mixture of benzyl alcohol and phenol in the presence of an effective amount of activated alumina as a catalyst.

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Chemical process for preparing di-ortho benzyl phenols

TL;DR: Phenols having an unsubstituted ortho-position are benzylated by reaction with a benzyl alcohol in contact with an activated alumina catalyst especially gamma alumina at a temperature sufficient to maintain the reactants in the vapor phase as mentioned in this paper.
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Process for the monobenzylation of p-substituted phenols

TL;DR: In this article, a process for the preparation of p-substituted o-benzylphenols by reaction of psubstitized phenols with optionally substituted benzyl halides, benzyl esters or benzyl ethers in the presence of an acid catalyst at elevated temperature in a distillation column is described.
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Production of o-benzylphenol

TL;DR: In this article, a method to produce a titled compound useful as a synthetic intermediate of organic compounds, especially pharmaceuticals, suppressing the production of by-products, by adding benzyl alcohol to phenol containing a catalyst, and reacting the components.
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Aromatic coupling process

TL;DR: In this article, 4-(2-Cyano-4-nitrophenyl)phenols are prepared by reacting a 3-cyano-1-nitrobenzene having a replaceable hydrogen in the 4-position with a phenol having a replacement in the position in an inert solvent and in the presence of a strong base.
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Method of making benzylated phenols

TL;DR: In this article, a method of making benzylated phenols comprises contacting a phenol and a benzyl alcohol with a basic metal oxide catalyst at a temperature sufficient to maintain each of the phenol in a vapor phase.
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Journal ArticleDOI

Industrial and Engineering Chemistry

TL;DR: The American Chemical Society (ACS) as mentioned in this paper in 1941 received 878 manuscripts for consideration, including 13 symposia, some of them emphasized by the use of special inks in printing, decorative typographical devices, or extra illustration.
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Alkylation of phenols

TL;DR: In this paper, an improved method of alkylating phenols with alcohols containing less than six carbon atoms per molecule was proposed, which is referred to as tertiary butyl phenols.
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Alkylation of phenols

TL;DR: In this paper, the alkylation of phenols by reacting the latter with aliphatic ethers in the presence of suitable condensation and dehydration agents is described. But the method of producing alkylated phenols is not described.