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347825

Sigma-Aldrich

Potassium carbonate

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

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About This Item

Linear Formula:
K2CO3
CAS Number:
584-08-7
Molecular Weight:
138.21
Beilstein/REAXYS Number:
4267587
EC Number:
209-529-3
MDL number:
MFCD00011382
UNSPSC Code:
12352302
PubChem Substance ID:
329755057
NACRES:
NA.21

grade

reagent grade

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
GHS07

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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 using palladium complexed to dendrimers on silica.
Alper H, et al.
Canadian Journal of Chemistry, 78(6), 920-924 (2000)
Carlos Arroniz et al.
Organic letters, 15(4), 910-913 (2013-02-05)
ortho-Arylation of ortho-substituted benzoic acids is a challenging process due to the tendency of the reaction products toward Pd-catalyzed protodecarboxylation. A simple method for preventing decarboxylation in sterically hindered benzoic acids is reported. The method described represents a reliable and
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