Polidoro, Daniele et al. published their research in ACS Sustainable Chemistry & Engineering in 2022 |CAS: 585-88-6

The Article related to hydrogenation glucosamine acetylglucosamine glucose maltose ruthenium carbon catalyst, Industrial Organic Chemicals, Leather, Fats, and Waxes: Manufacture Of Industrial Organic Chemicals and other aspects.Name: SweetPearlR P300 DC Maltitol

On February 28, 2022, Polidoro, Daniele; Perosa, Alvise; Barbaro, Elena; Feltracco, Matteo; Argiriadis, Elena; Selva, Maurizio published an article.Name: SweetPearlR P300 DC Maltitol The title of the article was Multiphase Hydrogenation of D-Glucosamine Hydrochloride, N-Acetyl-D-Glucosamine, D-Glucose, and D-Maltose over Ru/C with Integrated Catalyst Recovery. And the article contained the following:

A multiphase (MP) system composed of two immiscible liquids, water and isooctane, and com. 5% Ru/C as a catalyst, both with and without an addnl. organic liquid (OL: THF, 2-methyl-THF, Me iso-Bu carbinol, and cyclopentyl Me ether) was designed and investigated for the chemoselective catalytic hydrogenation of four model examples of biobased sugars and amino/amido-sugars. At 110°C and 40 bar of H2, D-glucosamine hydrochloride and N-acetyl-D-glucosamine were converted selectively into their corresponding hydrogenated derivatives, 2-amino-D-sorbitol and 2-acetamide-D-sorbitol, resp., isolated in >99% yields. Both the reagents and the products were converted and formed in the aqueous phase, resp., while, by tuning the relative proportions of water, isooctane, and the third added liquid (particularly THF), the catalyst (Ru/C) was perfectly segregated in the organic layer, where it could be recycled and reused up to nine times without any loss of activity and selectivity, in a semicontinuous mode. Under such conditions, the reaction was implemented on a gram scale with a productivity up to 0.89 mmol 2-amino-D-sorbitol/(gcat h). The same hydrogenation efficiency and reagent/product/catalyst separation were achieved during the MP reactions of D-glucose and D-maltose. In this case, however, results were independent of the MP composition: at 120°C and 20-40 bar of H2, using either H2O/isooctane or H2O/isooctane/OL systems, a quant. conversion of D-glucose and D-maltose was reached with a selectivity up to 78 and >99% toward sorbitol and maltitol, resp. Ru/C was perfectly separated out of the aqueous phase in both MP mixtures, with a negligible metal leaching, below 0.01 weight %. The multiphase approach for all the tested substrates proved not only to be an original and robust protocol to improve the product isolation and catalyst recycling, but also effective in preventing metal contamination in the synthesis of final derivatives The experimental process involved the reaction of SweetPearlR P300 DC Maltitol(cas: 585-88-6).Name: SweetPearlR P300 DC Maltitol

The Article related to hydrogenation glucosamine acetylglucosamine glucose maltose ruthenium carbon catalyst, Industrial Organic Chemicals, Leather, Fats, and Waxes: Manufacture Of Industrial Organic Chemicals and other aspects.Name: SweetPearlR P300 DC Maltitol

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