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通过环糊精介导的氢甲酰化反应在水中从植物油连续生产双功能平台化学品

Continuous Production of Bifunctional Platform Chemicals From Plant Oils in Water by Cyclodextrin-Mediated Hydroformylation.

作者信息

Roth Thomas Friedrich Hubertus, Averbeck Tobias, Daalmann Marvin, Vogt Dieter, Seidensticker Thomas

机构信息

TU Dortmund University, Department for Biochemical and Chemical Engineering, Laboratory of Industrial Chemistry, Emil-Figge-Straße 66, 44227, Dortmund, Germany.

出版信息

ChemSusChem. 2025 May 19;18(10):e202402421. doi: 10.1002/cssc.202402421. Epub 2025 Jan 23.

Abstract

Platform chemicals from renewable resources with broad applications are highly desirable, particularly for replacing fossil-based monomers. Bifunctional aliphatic ester-aldehydes, accessible via regioselective hydroformylation of unsaturated oleochemicals, can be converted into linear ω-amino/ω-hydroxy esters and dicarboxylic acids-key building blocks for biobased aliphatic polycondensates. However, their success hinges on efficient, economically viable production, with catalyst recycling being critical. We present the Rh-catalyzed, cyclodextrin-mediated, aqueous biphasic hydroformylation of methyl 10-undecenoate (from castor oil) and methyl 9-decenoate (from rapeseed oil) to produce methyl 12-oxododecanoate and methyl 11-oxoundecanoate, respectively, with high yields and productivity. This system allows for efficient catalyst recycling via decantation, maintaining 30 % of its native activity in aqueous biphasic conditions. Reaction conditions were optimized using a tailored experimental design, reducing nearly 200 experiments to 39 without sacrificing predictive accuracy. The optimized conditions were transferred to a continuous miniplant, achieving a low rhodium loss of 0.018 % h, with excellent space-time yields of 76.5 kg h m. Rhodium in the product was as low as 79 ppb, with 4.4 kg of product per mg of catalyst lost, marking a significant step in combining hydroformylation-derived, bio-based platform chemicals with economic industrial potential.

摘要

具有广泛应用的来自可再生资源的平台化学品非常受欢迎,特别是用于替代基于化石的单体。通过不饱和油脂化学物质的区域选择性氢甲酰化可获得的双功能脂肪族酯醛,可以转化为线性ω-氨基/ω-羟基酯和二羧酸——生物基脂肪族缩聚物的关键构建块。然而,它们的成功取决于高效、经济可行的生产,其中催化剂循环利用至关重要。我们展示了铑催化、环糊精介导的10-十一烯酸甲酯(来自蓖麻油)和9-癸烯酸甲酯(来自菜籽油)的水相双相氢甲酰化反应,分别高产率和高生产力地生成12-氧代十二烷酸甲酯和11-氧代十一烷酸甲酯。该体系允许通过倾析进行高效的催化剂循环利用,在水相双相条件下保持其原始活性的30%。使用定制的实验设计对反应条件进行了优化,将近200次实验减少到39次,同时不牺牲预测准确性。优化后的条件被转移到连续微型工厂,实现了0.018% h的低铑损失,时空产率高达76.5 kg h m 。产品中的铑含量低至79 ppb,每毫克催化剂损失4.4 kg产品,这标志着将氢甲酰化衍生的、具有经济工业潜力的生物基平台化学品相结合方面迈出了重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f1/12094140/74de19ebd71b/CSSC-18-e202402421-g002.jpg

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