Synthesis of acetic acid and acetic anhydride from methanol carbonylation with polymer supported rhodium catalyst

2008 ◽  
Vol 9 (5) ◽  
pp. 853-858 ◽  
Author(s):  
Shufeng Zhang ◽  
Cunyue Guo ◽  
Qingli Qian ◽  
Guoqing Yuan
ChemInform ◽  
2000 ◽  
Vol 31 (40) ◽  
pp. no-no
Author(s):  
Rebecca A. Taylor ◽  
Brian P. Santora ◽  
Michel R. Gagne

2000 ◽  
Vol 2 (12) ◽  
pp. 1781-1783 ◽  
Author(s):  
Rebecca A. Taylor ◽  
Brian P. Santora ◽  
Michel R. Gagné

2019 ◽  
Vol 55 (91) ◽  
pp. 13721-13724 ◽  
Author(s):  
Zuyu Liang ◽  
Jianbin Chen ◽  
Xin Chen ◽  
Kai Zhang ◽  
Jinhe Lv ◽  
...  

A novel porous organic polymer supported rhodium catalyst (Rh/POL-BINAPa&PPh3) was developed for the hydroformylation of alkynes to afford α,β-unsaturated aldehydes.


1991 ◽  
Vol 56 (12) ◽  
pp. 2917-2935 ◽  
Author(s):  
Eva Klinotová ◽  
Václav Křeček ◽  
Jiří Klinot ◽  
Miloš Buděšínský ◽  
Jaroslav Podlaha ◽  
...  

3β-Acetoxy-21,22-dioxo-18α,19βH-ursan-28,20β-olide (IIIa) reacts with acetic anhydride in pyridine under very mild conditions affording β-lactone IVa and γ-lactones Va and VIIa as condensation products. On reaction with pyridine, lactones Va and VIIa undergo elimination of acetic acid to give unsaturated lactones VIIIa and IXa, respectively. Similarly, the condensation of 20β,28-epoxy-21,22-dioxo-18α,19βH-ursan-3β-yl acetate (IIIb) with acetic anhydride leads to β-lactone IVb and γ-lactone Vb; the latter on heating with pyridine affords unsaturated lactone VIIIb and 21-methylene-22-ketone Xb. The structure of the obtained compounds was derived using spectral methods, particularly 1H and 13C NMR spectroscopy; structure of lactone IVa was confirmed by X-ray diffraction.


1988 ◽  
Vol 212 ◽  
pp. 73-79 ◽  
Author(s):  
V. Vajgand ◽  
R. Mihajlović ◽  
Lj. Mihajlović ◽  
V. Joksimović
Keyword(s):  

Author(s):  
Mousumi Chakraborty ◽  
Vaishali Umrigar ◽  
Parimal A. Parikh

The present study aims at assessing the effect of microwave irradiation against thermal heat on the production of N-acetyl-p-anisidine by acetylation of p-anisidine. The acetylation of p-anisidine under microwave irradiation produces N-acetyl-p-anisidine in shorter reaction times, which offers a benefit to the laboratories as well as industries. It also eliminates the use of excess solvent. Effects of operating parameters such as reaction time, feed composition, and microwave energy and reaction temperature on selectivity to the desired product have been investigated. The results indicate as high as a 98% conversion of N-acetyl-p-anisidine can be achieved within 12-15 minutes using acetic acid. The use of acetic acid as an acetylating agent against conventionally used acetic anhydride eliminates the handling of explosive acetic anhydride and also the energy intensive distillation step for separation of acetic acid. Organic solvent like acetic anhydride are not only hazardous to the environment, they are also expensive and flammable.


2009 ◽  
Vol 54 (5) ◽  
pp. 1610-1612 ◽  
Author(s):  
Norihito Hiyoshi ◽  
Yoshio Masuda ◽  
Osamu Sato ◽  
Aritomo Yamaguchi ◽  
Chandrashekhar V. Rode ◽  
...  

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