Application of Focused Microwaves to the Scale-Up of Solvent-Free Organic Reactions

2000 ◽  
Vol 4 (6) ◽  
pp. 498-504 ◽  
Author(s):  
J. Cléophax ◽  
M. Liagre ◽  
A. Loupy ◽  
A. Petit
2020 ◽  
Author(s):  
Amy Frankhouser ◽  
Matthew Kanan

<div><div><div><p>A solvent-free transformation that enables production of polyester precursors from inedible biomass proceeds from a heterogeneous reaction mixture containing both solid and molten components. Characterization of the evolution of these component phases over the course of the reaction provides insight relevant to process design and scale-up.</p></div></div></div>


1991 ◽  
Vol 69 (1) ◽  
pp. 116-120 ◽  
Author(s):  
M. J. Kirk ◽  
T. S. Sorensen

The organic reactions that take place during the thermal coking of bitumen are extremely complex and deep-seated, but obviously hydrogen atoms originally attached to carbons that form coke will have moved to a new carbon site (net addition of hydrogen, resulting in upgraded bitumen). Accompanying this process, one expects some general hydrogen shuttling between non-coking molecules. This paper describes an approach to determing the extent of this latter process by the addition of a small amount of perdeuterated pyrene to the bitumen prior to the coking operation. The in situ pyrene functions as in indicator, allowing one to establish the extent and other mechanistic details of the "hydrogen donor" reactions that take place during coking. There is no indication that the pyrene substantially modifies the normal course of the reaction, hence the analogy to an indicator. Key words: bitumen coking, pyrene, hydrogen exchange, donor solvent, free radicals.


2008 ◽  
Vol 61 (6) ◽  
pp. 419 ◽  
Author(s):  
Matthew J. Spafford ◽  
James E. Christensen ◽  
Matthew G. Huddle ◽  
Joshua R. Lacey ◽  
Ram S. Mohan

A bismuth trifluoromethanesulfonate (triflate)-catalyzed (2.0 mol-%) multicomponent reaction involving the allylation of dioxolanes followed by in situ derivatization with anhydrides to generate highly functionalized esters has been developed under solvent-free conditions. Most reagents used to date for allylation of dioxolanes are highly corrosive and are often required in stoichiometric amounts. In contrast, the use of a relatively non-toxic and non-corrosive bismuth(iii)-based catalyst makes this methodology especially attractive for scale-up.


ChemInform ◽  
2010 ◽  
Vol 31 (34) ◽  
pp. no-no
Author(s):  
Massimo Gianotti ◽  
Giorgio Martelli ◽  
Giuseppe Spunta ◽  
Eileen Campana ◽  
Mauro Panunzio ◽  
...  

2017 ◽  
Vol 19 (6) ◽  
pp. 1507-1518 ◽  
Author(s):  
Deborah E. Crawford ◽  
Clodagh K. G. Miskimmin ◽  
Ahmad B. Albadarin ◽  
Gavin Walker ◽  
Stuart L. James

Several organic reactions have been achieved quantitatively without any added solvent, using solid or liquid reagents, on a continuous basis; products are typically obtained directly in analytically pure form, requiring no work-up.


2020 ◽  
Author(s):  
Amy Frankhouser ◽  
Matthew Kanan

<div><div><div><p>A solvent-free transformation that enables production of polyester precursors from inedible biomass proceeds from a heterogeneous reaction mixture containing both solid and molten components. Characterization of the evolution of these component phases over the course of the reaction provides insight relevant to process design and scale-up.</p></div></div></div>


ChemInform ◽  
2010 ◽  
Vol 30 (13) ◽  
pp. no-no
Author(s):  
Rajender S. Varma ◽  
Dalip Kumar ◽  
Rajender Dahiya ◽  
Per J. Liesen

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