Ethyl potassium malonate CAS 6148-64-7
Introduction：Basic information about Ethyl potassium malonate CAS 6148-64-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Ethyl potassium malonate Basic information
| Product Name: | Ethyl potassium malonate |
| Synonyms: | AKOS 310;MALONIC ACID MONOETHYL ESTER POTASSIUM SALT;ETHYL POTASSIUM MALONATE;ETHYL MALONATE MONOPOTASSIUM SALT;ETHYL MALONATE POTASSIUM SALT;ETHYL MONO POTASSIUM MALONATE;KEM;MALONIC ACID MONOETHYL ESTER POTASSIUM |
| CAS: | 6148-64-7 |
| MF: | C5H7KO4 |
| MW: | 170.2 |
| EINECS: | 228-156-7 |
| Product Categories: | Pharmaceutical Intermediates;bc0001;6148-64-7 |
| Mol File: | 6148-64-7.mol |
Ethyl potassium malonate Chemical Properties
| Melting point | 194 °C (dec.) (lit.) |
| storage temp. | Inert atmosphere,Room Temperature |
| solubility | Methanol (Slightly), Water (Slightly) |
| form | Powder or Cyrstals |
| color | White |
| PH | pH(50g/l, 25℃) : 5.5～8.0 |
| Water Solubility | soluble |
| Sensitive | Hygroscopic |
| BRN | 3721682 |
| InChI | InChI=1S/C5H8O4.K.H/c1-2-9-5(8)3-4(6)7;;/h2-3H2,1H3,(H,6,7);; |
| InChIKey | WVUCPRGADMCTBN-UHFFFAOYSA-M |
| SMILES | C(C(=O)O)C(=O)OCC.[KH] |
| CAS DataBase Reference | 6148-64-7(CAS DataBase Reference) |
Safety Information
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36-37/39 |
| WGK Germany | 2 |
| HS Code | 29171910 |
| Storage Class | 11 - Combustible Solids |
| Chemical Properties | white crystals or powder |
| Uses | Ethyl potassium malonate is used as a competitive inhibitor of the enzyme succinate dehydrogenase. It acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation. Further, it reacts with aryl nitriles to prepare beta-amino acrylates in the presence of zinc chloride and a catalytic amount of Hünig's base. In addition to this, it serves as an intermediate for the preparation of ethyl tert-butyl malonate. |
| Uses | Ethyl potassium malonate (potassium ethyl malonate) may be used to generate (trimethylsilyl)ethyl malonate in situ, which can be acylated to prepare a variety of β-ketoesters or alkylidene malonates. |
| General Description | Ethyl potassium malonate (potassium ethyl malonate) reacts with aryl nitriles in the presence of zinc chloride and a catalytic amount of Hünig′s base to yield β-amino acrylates. Ethyl potassium malonate is formed as an intermediate during the synthesis of ethyl tert-butyl malonate. |
| Synthesis | 105-53-3 6148-64-7 Step 1: Add diethyl malonate (100g, 0.625mol) and anhydrous ethanol (400ml) to a 2 liter round bottom flask fitted with a magnetic stirrer. A solution of potassium hydroxide (35 g, 0.624 mol) in anhydrous ethanol (400 ml) was slowly added dropwise at room temperature. After the dropwise addition, the reaction mixture was continued to be stirred overnight. Subsequently, the reaction mixture was heated to reflux and then slowly cooled to room temperature. The first products were isolated by vacuum filtration through a large No. 2 sintered glass funnel and dried at room temperature for 1 hour. The filtrate was concentrated to about 500 ml and then cooled to room temperature to precipitate the second batch of crystals. Combining the two batches of product, the total yield was 97.7 g with 92% yield. |
| References | [1] Patent: WO2012/25861, 2012, A1. Location in patent: Page/Page column 20 [2] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 18, p. 4995 - 5010 [3] Angewandte Chemie - International Edition, 2011, vol. 50, # 19, p. 4470 - 4474 [4] Chemistry - A European Journal, 2003, vol. 9, # 17, p. 4222 - 4231 [5] Tetrahedron, 2012, vol. 68, # 9, p. 2113 - 2120 |
Ethyl potassium malonate Preparation Products And Raw materials
| Raw materials | Ethanol-->Potassium hydroxide-->Ethyl hydrogen malonate-->Diethyl malonate |
| Preparation Products | Ethyl 2-chloropyrimidine-5-carboxylate-->2-MORPHOLIN-4-YL-PYRIMIDINE-5-CARBALDEHYDE-->ETHYL 2-HYDROXYPYRIMIDINE-5-CARBOXYLATE-->MONO-BENZYL MALONATE-->Ethyl 2,6-dichloro-5-fluoro-pyridine-3-acetoacetate-->3-CYCLOPROPYL-3-OXO-PROPIONIC ACID ETHYL ESTER-->ETHYL 3-METHOXYPHENYLACETATE-->Ethyl isobutyrylacetate-->3-OXO-3-(3-TRIFLUOROMETHYLPHENYL)PROPIONIC ACID ETHYL ESTER-->TERT-BUTYL 3-(ETHOXYCARBONYL)-2-OXOPROPYLCARBAMATE-->3-(4-TERT-BUTOXYCARBONYLAMINO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER |
