Examples of 'alkylation reaction' in a sentence
Meaning of "alkylation reaction"
In chemistry, an alkylation reaction refers to a chemical process in which an alkyl group (a group of atoms derived from an alkane) is added to a molecule. This reaction is commonly used to introduce alkyl groups into a compound and is widely utilized in organic synthesis
How to use "alkylation reaction" in a sentence
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alkylation reaction
A mechanism for the alkylation reaction is proposed.
The alkylation reaction is generally performed in a solvent.
Reaction conditions conducive to the alkylation reaction are employed.
Another alkylation reaction was performed using extraction.
This reaction has several advantages over the alkylation reaction.
The product of the alkylation reaction is an imine salt.
An alkylation reaction of such an acetale precursor moiety is particularly preferred.
Y is a leaving group in the alkylation reaction and is described below.
The alkylation reaction zone contains an alkylation catalyst.
Suitable agent for this alkylation reaction may include.
The alkylation reaction is well known.
The first one is based on a decarboxylative asymmetric allylic alkylation reaction.
A second alkylation reaction was run in the same manner.
A wide variety of catalysts can be used in the alkylation reaction zone.
This alkylation reaction is performed in the presence of a base.
See also
The useful solvents are solvents inert to the relevant alkylation reaction.
The alkylation reaction is carried out in the presence of a solvent.
The quantities of materials used in the alkylation reaction are based on the assay.
The alkylation reaction is carried out in the liquid phase.
The attached neutral polymer is then converted to a polyelectrolyte by an in situ alkylation reaction.
The alkylation reaction zone is operated in a predominantly liquid phase.
Branched chain olefins may be used as a feed source for an aromatic alkylation reaction.
The alkylation reaction can occur in any suitable solvent.
The resulting filtrate has a purity suitable for use in the alkylation reaction.
Following the alkylation reaction lysines were modified with succinic anhydride.
At least a portion of the second catalyst stream passes to the alkylation reaction zone.
The alkylation reaction is carried out in the presence of acidic catalysts.
The sulfuric acid present in the reaction zone serves as a catalyst to the alkylation reaction.
The direct alkylation reaction may be conducted in the presence of solvent.
The acid sludge may contain water and often comes from an alkylation reaction.
The alkylation reaction may be carried out batchwise or on a continuous basis.
Means for recycling said third cut at the entry of the alkylation reaction area.
This alkylation reaction is also conducted in the presence of an appropriate base.
The regeneration can be conducted together with the alkylation reaction in the same reactor.
An aromatic alkylation reaction uses olefins in an incoming stream to alkylate aromatic compounds.
Suitable solvents for the reaction include those listed above for the alkylation reaction.
The alkylation reaction and the redistribution reaction may occur concurrently.
The bromomethylcyclopropane typically contains an alkenyl impurity which can also participate in the alkylation reaction.
A suitable base used in the alkylation reaction is sodium hydroxide or sodium carbonate.
Enamines derived from piperidine can be used in the Stork enamine alkylation reaction.
The products of the alkylation reaction described include indanes and tetralins.
Olefinic and isobutane feedstocks are combined and mixed with HF in an alkylation reaction zone.
The alkylation reaction can be performed by techniques well known in the art.
The purity of the product of the alkylation reaction was confirmed by NMR spectroscopy.
The alkylation reaction can be designed to take place either continuously or batchwise.
Step 6 of the process comprises an alkylation reaction.
The direct alkylation reaction of step c may be carried out in several ways.
In some embodiments, this type of bond is formed by a reductive alkylation reaction.
The alkylation reaction is advantageously carried out in aprotic inert organic solvents.
In embodiments of the invention, the alkylation reaction is performed in a microwave.
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