(DIMETHYLAMINOMETHYLENE-AMINOMETHYLENE)DIMETHYLAMMONIUM CHLORIDE
(DIMETHYLAMINOMETHYLENE-AMINOMETHYLENE)DIMETHYLAMMONIUM CHLORIDE Basic information
- Product Name:
- (DIMETHYLAMINOMETHYLENE-AMINOMETHYLENE)DIMETHYLAMMONIUM CHLORIDE
- Synonyms:
-
- (DIMETHYLAMINOMETHYLENE-AMINOMETHYLENE)DIMETHYLAMMONIUM CHLORIDE
- [3-(DIMETHYLAMINO)-2-AZAPROP-2-EN-1-YLIDENE]DIMETHYLAMMONIUM CHLORIDE
- gold'S
- [3-(Dimethylamino)-2-azaprop-2-en-1-ylidene]dimethylammonium chloride, (Dimethylaminomethyleneaminomethylene)dimethylammonium chloride
- (([(Dimethylamino)methylidene]amino)methylidene)dimethylazanium chloride
- Gold's Reagent 95%
- Gold'sReagent>
- N-((((Dimethylamino)methylene)amino)methylene)-N-methylmethanaminium chloride
- CAS:
- 20353-93-9
- MF:
- C6H14ClN3
- MW:
- 163.65
- Mol File:
- 20353-93-9.mol
(DIMETHYLAMINOMETHYLENE-AMINOMETHYLENE)DIMETHYLAMMONIUM CHLORIDE Chemical Properties
- Melting point:
- 100-102 °C (lit.)
- solubility
- soluble in Methanol
- form
- powder to crystal
- color
- Light orange to Yellow to Green
- InChI
- InChI=1S/C6H14N3.ClH/c1-8(2)5-7-6-9(3)4;/h5-6H,1-4H3;1H/q+1;/p-1
- InChIKey
- DEIBXAPEZDJDRC-UHFFFAOYSA-M
- SMILES
- N(C)(C)/C=N/C=[N+](/C)\C.[Cl-]
MSDS
- Language:English Provider:SigmaAldrich
(DIMETHYLAMINOMETHYLENE-AMINOMETHYLENE)DIMETHYLAMMONIUM CHLORIDE Usage And Synthesis
Uses
Gold′s Reagent was used in the synthesis of 4-hydroxyquinazoline by reacting with ortho aminobenzoic acids.
Uses
[[[(Dimethylamino)methylene]amino]methylene]dimethylammonium Chloride is a β-dimethylaminomethylenating agent for ketones and amines; yields enamino derivatives of esters and lactones; converts Grignard reagents to aldehydes.
Synthesis
The Preparative Method of [[[(Dimethylamino)methylene]amino]methylene]dimethylammonium Chloride: a 1 L, one-necked, round-bottomed flask is equipped with a Claisen adapter, mechanical stirrer, reflux condenser, and mineral oil bubbler. The flask is charged with cyanuric chloride (73.8 g, 0.4 mol) (Caution: cyanuric chloride is a lachrymator and causes burns on contact with the skin), N,N-Dimethylformamide (175.4 g, 2.4 mol) and 1,4-dioxane (100 mL). The resulting solution is stirred and heated at 85 °C for 2-3 h while a considerable amount of carbon dioxide is evolved. When gas evolution is minimal, the reaction mixture is allowed to cool to room temperature; the product rapidly solidifies (eq 1). The flask which contains the solid product is connected to an isopropyl alcohol/dry ice trap and the solvent is removed by evacuating the system to approximately 0.05 mmHg. The crude product weighs 186-187 g (95% yield). Another method of isolating the product is by rapid filtration and washing with acetone.
Precautions
Gold's reagent is very hygroscopic and should be handled under a moisture-free environment. If kept dry, it has a substantial shelf-life. Store in desiccator over anhydrous calcium sulfate.
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