质量水平
产品线
ReagentPlus®
检测方案
99%
形式
solid
pH值（酸碱度）
11-13 (25 °C, 138 g/L)
mp
891 °C (lit.)
SMILES字符串
[K+].[K+].[O-]C([O-])=O
InChI
1S/CH2O3.2K/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
InChI key
BWHMMNNQKKPAPP-UHFFFAOYSA-L
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一般描述
Potassium carbonate is an inorganic base. It participates as a base in the palladacycle catalyzed Heck reaction of chlorobenzene with styrene. Addition of amino acids (glycine, sarcosine and proline) to K2CO3 (solvent) promotes the absorption of CO2.
应用
Potassium carbonate may be used in the following processes:
- As a reagent in the synthesis of polysubstituted iodobenzene derivatives.
- As a base for the Suzuki coupling of aryl halides with aryl boronic acids.
- The Heck reaction of styrene and bromobenzene.
- Preparation of disulfonated bis[4-(3-aminophenoxy)phenyl]sulfone, a disulfonated diamine monomer.
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
A kinetic study of CO2 capture with potassium carbonate solutions promoted with various amino acids: glycine, sarcosine and proline.
Thee H, et al.
International Journal of Greenhouse Gas Control, 20, 212-222 (2014)
Polyamide interfacial composite membranes prepared from m-phenylene diamine, trimesoyl chloride and a new disulfonated diamine.
Xie W, et al.
Journal of Membrane Science, 403, 152-161 (2012)
Robert Möckel et al.
Organic letters, 17(7), 1644-1647 (2015-03-21)
The cobalt-catalyzed Diels-Alder reaction of trimethylsilyl-substituted alkynes with 1,3-dienes led to dihydroaromatic intermediates which were transformed into iodobenzene derivatives. For this transformation, the dihydroaromatic intermediates had to be oxidized and the trimethylsilyl-substituted arene had to undergo a silicon-iodine exchange reaction.
Chelating N-heterocyclic carbene ligands in palladium-catalyzed Heck-type reactions.
Herrmann WA, et al.
Journal of Organometallic Chemistry, 557(1), 93-96 (1998)
Heck reaction catalyzed by phospha-palladacycles in non-aqueous ionic liquids.
Herrmann WA and Bohm VPW.
Journal of Organometallic Chemistry, 572(1), 141-145 (1999)
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