1994
DOI: 10.5650/jos1956.43.1089
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Addition Reaction of (+) -Limonene, 2-Pinene, and 2 (10) -Pinene with C1 C4 Alcohols in the Presence of Synthetic Zeolites

Abstract: Reactions of monoterpene hydrocarbons with alcohols (C1•`C4) were carried out in the presence of synthetic zeolites. The addition of (+)-limonene, 2-pinene, and 2 (10)-pinene to alcohols gave the corresponding terpenyl ethers as the major products. Some reaction products could be used as perfume bases.

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“…In this work, the heterogeneous catalysts were tested to be used for limonene alkoxylation. It is known that several zeolites with strong Bronsted acid sites are effective for this reaction [12][13][14].…”
Section: Limonene Etherificationmentioning
confidence: 99%
“…In this work, the heterogeneous catalysts were tested to be used for limonene alkoxylation. It is known that several zeolites with strong Bronsted acid sites are effective for this reaction [12][13][14].…”
Section: Limonene Etherificationmentioning
confidence: 99%
“…bZeolite is a large pore 12-ring zeolite with a three-dimensional system of channels, which selectively catalyzes the addition of methanol to the double bond of limonene [7][8][9][10]. This paper describes limonene enrichment from tire pyrolysis oil distillation and continuous limonene etherification by reacting limonene-enriched distillation fractions with methanol using a continuous microreactor.…”
Section: Introductionmentioning
confidence: 99%