Potassium hydride

Preparation

Preparation of a dipyrazolylborate -K[(C3N2H3)2BC8H14].
[(C3N2H3)2BC8H14]－ (abbreviated as Pz2BBN) is a bidentate ligand used to prepare catalysts with hydrogen-bonding capabilities, and has potential applications. However, the currently reported methods for preparing this ligand are not easy to industrialize. Therefore, developing a method that is easy to industrialize is of great significance for further expanding the application of this ligand.
The key points of the technical solution are: under anhydrous and oxygen-free conditions, 9-boron bicyclic [3.3.1]nonane dimer, potassium hydride, and pyrazole are reacted under stirring and reflux in anhydrous toluene or anhydrous tetrahydrofuran to prepare dipyrazolylborate -K[(C3N2H3)2BC8H14]. Using 9-boronbicyclo[3.3.1]nonane dimer, pyrazole, and potassium hydride as raw materials, dipyrazolyl borate -K[(C3N2H3)2BC8H14] was prepared by a one-step synthesis method. The role of H- is the same as that of OH- reported in the literature, but the product after combination with H+ is H2 instead of H2O, thus eliminating the need for dehydration. Furthermore, this invention also features short reaction time, fewer types of solvents required that can be recycled and reused, simple method, high product purity, low production cost, and ease of large-scale production.

Chemical Properties

Potassium hydride is available in laboratory quantities only as a 20 – 35 % dispersion in oil. Potassium hydride is a considerably stronger base than lithium hydride or sodium hydride. It is able to remove protons from tertiary alcohols and ketones, a reaction that either does not occur or is very slow when sodium hydride is used. Potassium hydride also reacts with weak Lewis acids, converting sterically hindered boron trialkyls to the corresponding sterically hindered complex borohydrides:

Uses

Organic condensations and alkylations.

Uses

Potassium Hydride is used in preparation of Hydroxy-Xanthone derivatives via Isoprenylation followed by Claisen rearrangement starting from Fluoroxanthone derivatives.

Uses

It is used as a strong reducing agent and inmaking super bases RNHK and ROK(whereRis an alkyl group) (Sullivan andWade 1980).It is sold as 35 wt% dispersion in mineral oil.

Definition

potassium hydride: A white orgreyish white crystalline solid, KH;r.d. 1.43–1.47. It is prepared by passinghydrogen over heated potassiumand marketed as a light grey powderdispersed in oil. The solid decomposeson heating and in contact withmoisture and is an excellent reducingagent. Potassium hydride is a firehazard because it produces hydrogenon reaction with water.

Reactions

Potassium hydride acts as a base and as hydride donor. It is used for deprotonation, cyclization-condensation, elimination, and rearrangement reactions, and also as a reducing agent. Potassium hydride undergoes reaction quickly and quantitatively with acids, and of particular note is its capability to rapidly deprotonate tertiary alcohols where sodium hydride or potassium metal do so slowly or not at all. The reactions of metal hydrides take place at the crystal surface. The crystal lattice energies decrease from lithium to cesium hydride, and potassium hydride appears to have the optimal lattice energy and hydride radius for surface reactions. The presence of 18-crown-6 enhances the reactivity of potassium hydride, The crown ether can operate as a phase-transfer agent or as a simple “pickling” agent of the potassium hydride surface, dissolving the formed inorganic salts. Potassium hydride is usually superior to lithium and sodium hydride in the reactions. Unusually active potassium hydride can be prepared easily from hydrogen and superbasic reagents (t-BuOK-TMEDA) in hexane. “Superactive potassium hydride” is very active in deprotonation as well as in reduction. The reactivity of commercially available potassium hydride, which is prepared by the reaction of hydrogen gas with elemental potassium, depends upon the impurities in different lots (mainly potassium or its reaction products), thus leading to side reactions and variable yields. The superactive metal hydride contains no alkali metal.

General Description

This product has been enhanced for energy efficiency.

Hazard

Dangerous fire and explosion risk, evolves toxic and flammable gases on heating and on expo- sure to moisture.

Health Hazard

The toxicity data on potassium hydride arenot reported in the literature. In the pure state, this compound should be highly corrosiveby inhalation, ingestion, and skin contact.It yields potassium hydroxide, whichis also very corrosive, when reacted withmoisture.

Health Hazard

Potassium hydride react with the moisture on skin and other tissues to form highly corrosive sodium and potassium hydroxide. Contact of these hydrides with the skin, eyes, or mucous membranes causes severe burns; thermal burns may also occur due to ignition of the liberated hydrogen gas.

Fire Hazard

Potassium hydride is flammable solid that ignite on contact with moist air. Potassium hydride presents a more serious fire hazard than sodium hydride. The mineral oil dispersions do not ignite spontaneously on exposure to the atmosphere. Sodium hydride and potassium hydride fires must be extinguished with a class D dry chemical extinguisher or by the use of sand, ground limestone, dry clay or graphite, or "Met-L-X " type solids. Water or CO 2 extinguishers must never be used on sodium and potassium hydride fires.

Flammability and Explosibility

Potassium hydride and sodium hydride are flammable solids that ignite on contact with moist air. Potassium hydride presents a more serious fire hazard than sodium hydride. The mineral oil dispersions do not ignite spontaneously on exposure to the atmosphere. Sodium hydride and potassium hydride fires must be extinguished with a class D dry chemical extinguisher or by the use of sand, ground limestone, dry clay or graphite, or "Met-L-X" type solids. Water or CO2 extinguishers must never be used on sodium and potassium hydride fires.

reaction suitability

reagent type: reductant

Safety Profile

Dangerous fire hazard by chemical reaction. Ignites spontaneously in air. Moderate explosion hazard when exposed to heat or by chemical reaction. Wdl react with water, steam, or acids to produce H2 which then igmtes. Can react vigorously with oxidizing materials. To fight fire, use CO2, dry chemical. Potentially explosive reactions with 0-2,4- dnitrophenylhydroxylamine, fluoroalkenes. Ignites on contact with air, oxygen + moisture, fluorine. Incompatible with Cl2, acetic acid, acrolein, acrylonitrile, (CaC + Cl2), ClO2, (H202 + Cl2), (CHFL + CH,OH), 1,2-dchloroethylene, maleic anhydride, (n-methyl-n-nitrosourea + CH2Cl2), nitroethane, NCb, nitromethane, nitroparaffins, o-nitrophenol, nitropropane, n-nitrosomethylurea, (nitrosomethylurea + CH2Cl2), H20, trichloroethylene, tetrahydrofuran, tetrachlorethane. When heated to decomposition it emits highly toxic fumes of K2O. See also POTASSIUM and HYDRIDES.

storage

Safety glasses, impermeable gloves, and a fire-retardant laboratory coat should be worn at all times when working with these substances. These hydrides should be used only in areas free of ignition sources and should be stored preferably as mineral oil dispersions under an inert gas such as argon.

Incompatibilities

Potassium hydride and sodium hydride react violently with water, liberating hydrogen, which can ignite. Oil dispersions of these hydrides are much safer to handle because the mineral oil serves as a barrier to moisture and air. Potassium hydride may react violently with oxygen, CO, dimethyl sulfoxide, alcohols, and acids. Explosions can result from contact of these compounds with strong oxidizers. Potassium hydride is generally more reactive than sodium hydride.

Waste Disposal

Excess potassium or sodium hydride and waste material containing these substances should be placed in an appropriate container under an inert atmosphere, clearly labeled, and handled according to your institution's waste disposal guidelines. Experienced personnel can destroy small quantities of sodium hydride and potassium hydride by the careful dropwise addition of t-butanol or iso-propanol to a suspension of the metal hydride in an inert solvent such as toluene under an inert atmosphere such as argon. Great care must be taken in the destruction of potassium hydride because of its greater reactivity. The resulting mixture of metal alkoxide should be placed in an appropriate container, clearly labeled, and handled according to your institution's waste disposal guidelines.