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Merck

347825

Sigma-Aldrich

Potassium carbonate

reagent grade, ≥98%, powder, −325 mesh

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About This Item

Fórmula lineal:
K2CO3
Número de CAS:
Peso molecular:
138.21
Beilstein/REAXYS Number:
4267587
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21

grade

reagent grade

Quality Level

assay

≥98%

form

powder

particle size

−325 mesh

pH

11-13 (25 °C, 138 g/L)

mp

891 °C (lit.)

SMILES string

[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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General description

Potassium carbonate is an inorganic base. It participates as base in the palladacycle catalyzed Heck reaction of chlorobenzene with styrene.

Application

Potassium carbonate was used in the following studies:
  • Synthesis of polysubstituted iodobenzene derivatives.
  • As base for the synthesis of high molecular weight homopolymers and copolymers derived from various bisphenols.
  • As base for the Suzuki coupling of aryl halides with aryl boronic acids.
  • As base for the Heck reaction of styrene and bromobenzene.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Heck reaction using palladium complexed to dendrimers on silica.
Alper H, et al.
Canadian Journal of Chemistry, 78(6), 920-924 (2000)
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.
Synthesis, kinetic observations and characteristics of polyarylene ether sulphones prepared via a potassium carbonate DMAC process.
Viswanathan R, et al.
Polymer, 25(12), 1827-1836 (1984)
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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