2144-40-3Relevant articles and documents
A highly efficient procedure for ruthenium tetroxide catalyzed oxidative cyclizations of 1,5-dienes
Roth, Stefanie,Goehler, Sabrina,Cheng, Huan,Stark, Christian B. W.
, p. 4109 - 4118 (2005)
We report a highly efficient procedure for the oxidative cyclization of 1,5-dienes, which generally allows for high yields and selectivities. A solid-supported terminal oxidant and a finely tuned solvent mixture have both been identified as critical facto
Perruthenate ion. Another metal oxo species able to promote the oxidative cyclisation of 1,5-dienes to 2,5-disubstituted cis-tetrahydrofurans
Piccialli, Vincenzo,Caserta, Teresa
, p. 303 - 308 (2004)
Perruthenate ion, from tetrapropylammonium perruthenate (TPAP), in the presence of tetrabutylammonium periodate (TBAPI) as reoxidant catalyses the stereospecific and stereoselective oxidative cyclisation of 1,5-dienes to cis-2,5-disubstituted tetrahydrofu
Preparation method 2 and 5 - tetrahydrofuran dimethanol
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Paragraph 0072-0106, (2021/11/19)
The preparation method of 2-5 - tetrahydrofuran dimethanol (THFDM) comprises the following steps: mixing a solvent containing 5 - hydroxymethylfurfural raw material with a catalyst, and reacting in an atmosphere containing hydrogen to obtain the 2 and 5 - tetrahydrofuran dimethanol. The purity of 5 - hydroxymethyl furfural raw material is 90 - 99%. The catalyst comprises a carrier and an active component. The active component is loaded on the carrier. The active component includes a noble metal element. The carrier comprises a carbon material. The method is simple in synthesis process, and has a great application prospect in the field of a plurality of fields, especially degradable materials.
Highly selective ring rearrangement of 5-hydroxymethylfurfural to 3-hydroxymethylcyclopentanon catalyzed by non-noble Ni-Fe/Al2O3
Li, Jiachen,Feng, Yunchao,Wang, Huiqiang,Tang, Xing,Sun, Yong,Zeng, Xianhai,Lin, Lu
, (2021/03/14)
3-Hydroxymethylcyclopentanone (HCPN) has been regarded as a considerable intermediate for the synthesis of polymers, pesticides and fragrances, which is mainly produced from petrochemical refinery. In recent years, the preparation of HCPN from biomass has gradually attracted attention. HCPN can be obtained through the selective ring rearrangement of biomass-based 5-hydroxymethyl furfural (5-HMF). In this paper, the Ni-Fe/Al2O3 was fabricated and used as an efficient catalyst for the production of HCPN, giving a 5-HMF complete conversion with a high HCPN selectivity (86 %) at 160 °C under 4 MPa H2 for 4 h. The optimized Ni-Fe/Al2O3 showed excellent activity towards the production of HCPN compared with monometallic catalysts, suggesting that there was a synergistic effect in Ni-Fe alloy. The introduction of Fe into Ni/Al2O3 improved the H2 adsorption capacity and also changed the acidic/basic sites, which are beneficial for the formation of HCPN. Moreover, Ni-Fe/Al2O3 exhibited superb stability and could be successively used four times without obvious loss in catalytic activity.
Highly Controllable Hydrogenative Ring Rearrangement and Complete Hydrogenation Of Biobased Furfurals over Pd/La2B2O7 (B=Ti, Zr, Ce)
Tong, Zhikun,Gao, Rui,Li, Xiang,Guo, Lingyun,Wang, Jun,Zeng, Zheling,Deng, Qiang,Deng, Shuguang
, p. 4549 - 4556 (2021/09/09)
Developing a highly selective catalyst to upgrade furfurals (5-hydroxymethyl furfural and furfural) to cyclopentanones (3-hydroxymethyl cyclopentanone and cyclopentanone) and tetrahydrofuran alcohols (2,5-bishydroxymethyl tetrahydrofuran and tetrahydrofuran alcohol) is highly significant for biobased fine chemical synthesis. Here, a series of La2B2O7 (B=Ti, Zr, Ce) metal oxides, featuring the same chemical formula but different topological structures are fabricated. After Pd loading, the Lewis acidity and metal-support interaction are well governed by the support type, which further affects the hydrogenation and acid-catalyzed ability. A greater than 82 % yield of cyclopentanones is obtained via a hydrogenative ring rearrangement route over Pd/La2Ti2O7. However, Pd/La2Ce2O7 shows high catalytic efficiency for tetrahydrofuran alcohols with an approximately 80 % yield via a complete hydrogenation route. Additionally, the catalyst exhibits outstanding recycling performance and structural stability. This study presents an interesting design strategy for the selective preparation of cyclopentanones and tetrahydrofuran alcohols through the regulation of the adsorption mechanism.
