15467-25-1Relevant articles and documents
The synthesis of butene glycol ethers with aluminium triflate
Terblans, Yvette M.,Huyser, Michelle,Young, Desmond A.,Green, Michael J.
, p. 859 - 866 (2006)
The use of aluminium triflate as a ring-opening catalyst for butene oxide (BuO) was evaluated in the presence of different alcohols such as methanol, ethanol, n-propanol, n-butanol, 2-propanol, 2-methyl-1-propanol, and 2-methyl-2-propanol. The reaction with methanol was studied kinetically by varying the temperature, catalyst concentration, and methanol - butene oxide molar ratio. These reactions yielded two major products (2-methoxy-1-butanol and 1-methoxy-2-butanol) in a approximate ratio of 1:1. It was noted that at low catalyst concentrations (5 ppm), low temperatures (90 °C), and a MeOH-BuO molar ratio of 8:1, the selectivity of the reaction could be kinetically manipulated to shift the product ratio towards 1-methoxy-2-butanol, the α-alkoxyalcohol. This result was confirmed by an experimental design program. Statistical calculations using the data from the experimental design identified a feasible region in which reactions with methanol could be carried out, which would lead to slightly higher selectivities to 1-methoxy-2-butanol. This region shows that the methanol - butene oxide ratio should be 8:1, the temperature between 80 and 85 °C, and the catalyst concentration between 3.9 and 5 ppm. These reaction conditions were used to carry out a test reaction with methanol and an extended series of alcohols. All the alcohols, except for 2-methyl-2-propanol, reacted with butene oxide under these conditions, with the selectivity to the α-alkoxyalcohol higher than to the β- alkoxyalcohol. To obtain a ring-opening reaction with 2-methyl-2-propanol, it was found that a higher catalyst concentration (approximately 10 ppm) and a lower alcohol - butene oxide ratio (6:1) at a temperature of 80 °C were necessary. This reaction led to a mixture of 1-tert-butoxy-2-butanol and 2-tert-butoxy-1-butanol with the selectivity to the α-alkoxyalcohol being somewhat higher because of the steric influence of the bulky tert-butoxy group.
Polyoxometalate-modified reduced graphene oxide foam as a monolith reactor for efficient flow catalysis of epoxide ring-opening reactions
Jing, Xiaoting,Li, Zhen,Geng, Weijie,Lv, Hongjin,Chi, Yingnan,Hu, Changwen
, p. 8480 - 8488 (2021/04/12)
Continuous flow catalysis has been attracting significant interest due to its remarkable advantages over traditional batch reactions. In this work, a facile and broad-spectrum hydrothermal approach has been developed to construct polyoxometalate-modified reduced graphene oxide (POM@rGO) foam, which worked as a monolith reactor for efficient continuous flow catalysis of epoxide ring-opening reactions. The porous structures of rGO foam allow the high dispersion of the POM catalyst onto the substrate through electrostatic interactions. Specifically, a phosphotungstic acid (H3PW12O40, denoted as PW12)-modified rGO (PW12@rGO) monolith reactor exhibits remarkable catalytic activity and durability towards epoxide ring-opening reactions with alcohols, achieving 99% conversion and 92% selectivity for the methanolysis product in 10 min under ambient conditions without stirring. Notably, while coupling with a micro-injection pump, such PW12@rGO foam can work as an efficient continuous flow reactor towards methanolysis of styrene oxide for 38 h with 99% conversion and over 90% selectivity, reaching a turnover number (TON) as high as 28?044.
Graphite oxide: A simple and efficient solid acid catalyst for the ring-opening of epoxides by alcohols
Mirza-Aghayan, Maryam,Alizadeh, Mahdi,Molaee Tavana, Mahdieh,Boukherroub, Rabah
, p. 6694 - 6697 (2014/12/11)
A simple, efficient, and general procedure for the ring-opening of epoxides with various alcohols to give the corresponding β-alkoxy alcohols using graphite oxide (GO) as the catalyst, under very mild reaction conditions is described. The method proceeds in good to excellent yields and in short reaction times at room temperature under metal-free conditions.
