Examples of 'm-chloroperbenzoic' in a sentence
Meaning of "m-chloroperbenzoic"
m-chloroperbenzoic: relating to a chemical compound derived from benzoic acid and used as an oxidizing agent in organic synthesis
How to use "m-chloroperbenzoic" in a sentence
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m-chloroperbenzoic
The term mcpba means m-chloroperbenzoic acid.
M-chloroperbenzoic acid is convenient because generally it reacts comparatively rapidly to produce an N-oxide.
Typical oxidizing agents include m-chloroperbenzoic acid.
Expensiveness of m-chloroperbenzoic acid is an additional problem.
The oxidating agent is preferably m-chloroperbenzoic acid.
M-Chloroperbenzoic acid is highly explosive and is not preferable for industrial processes.
The oxidizing agent of choice is m-chloroperbenzoic acid.
Furthermore, m-chloroperbenzoic acid is expensive and poses an economic problem.
The most preferred epoxidation agent is m-chloroperbenzoic acid.
G of m-chloroperbenzoic acid are added in portions over 2 hours reaction time.
It is preferable to use m-chloroperbenzoic acid therefor.
Sulfides may be oxidized to sulfoxides and sulfones with reagents such as m-chloroperbenzoic acid.
Sulfoxides are preferably prepared using m-chloroperbenzoic acid according to standard methods.
However, m-chloroperbenzoic acid is preferred because of its high stability.
The preferred oxidant is m-chloroperbenzoic acid.
See also
Of m-Chloroperbenzoic acid in 200 ml of methylene chloride was stirred for 3 days at room temperature.
An example of the oxidant is m-chloroperbenzoic acid.
The oxidizing agent m-chloroperbenzoic acid ( or m-CPBA ) is a second grade poison.
The oxidizing agent of the invention is preferably m-chloroperbenzoic acid.
Examples of the peroxide include m-chloroperbenzoic acid, aqueous hydrogen peroxide, peracetic acid.
A particularly convenient reagent for this purpose is m-chloroperbenzoic acid.
Oxidizing agents include hydrogen peroxide, m-chloroperbenzoic acid peracetic acid, or magnesium monoperoxyphthalate.
Compound VI is oxidized to compound XIII with two equivalent of m-chloroperbenzoic acid.
The oxidizing agent is peracids such as m-chloroperbenzoic acid and so on ; and hydrogen peroxide.
The method as defined in claim 1, wherein the peroxy acid is m-chloroperbenzoic acid.
Peracetic acid, perbenzoic acid, m-chloroperbenzoic acid and perphthalic acid.
Next, ( 2 ) an oxygen atom is introduced thereto with the use of m-chloroperbenzoic acid.
Hydrogen peroxide, perbenzoic acid, m-chloroperbenzoic acid, or the like is used as an oxidizing agent.
The most preferred oxidizing agent is usually m-chloroperbenzoic acid.
Examples of the oxidant include m-chloroperbenzoic acid, peracetic acid, and a hydrogen peroxide solution.
Among others, hydrogen peroxide solution, perbenzoic acid, or m-chloroperbenzoic acid is preferred.
As the oxidizing agent, m-chloroperbenzoic acid, peracetic acid, hydrogen peroxide, etc . may be mentioned.
Converting the acetonide to an epoxide by reaction with m-chloroperbenzoic acid in methylene chloride ;.
Further, 10mg of m-chloroperbenzoic acid was added thereto, followed by stirring for 2 hours under ice-cooling.
Other oxidizing agents commonly used are m-chloroperbenzoic acid and triethylamine oxide.
Of these, m-chloroperbenzoic acid, Oxone ( registered trademark ), Dess-Martin periodinane are preferable.
This oil was dissolved in dichloromethane and m-chloroperbenzoic acid added portion-wise.
Sodium bicarbonate and m-chloroperbenzoic acid are used in amounts of 3 to 8 equivalents based on Compound ( R-2 ).
Examples of the peracid to be used herein are m-chloroperbenzoic acid and peracetic acid.
Resulting reaction mixture was at 0°C stirred during 120 minutes followed by precipitation of excess m-chloroperbenzoic acid.
Examples of the oxidizing agent include m-chloroperbenzoic acid, sodium periodate and the like.
After stirring at room temperature for 2 hours a further quantity of m-chloroperbenzoic acid ( 0.5g ) was added.
Examples of the oxidizing agent include m-chloroperbenzoic acid, sodium methaperiodate, hydrogen peroxide and the like.
N-substituted isatoic anhydrides VIII are obtained by treating VII with m-chloroperbenzoic acid ( m-CPBA ).
Thereto was added 900 mg of m-chloroperbenzoic acid at room temperature.
Oxidizing agents usable herein include, for example, perbenzoic acid, m-chloroperbenzoic acid, and peracetic acid.
Peracetic acid, perbenzoic acid, m-chloroperbenzoic acid, perphthalic acid, etc.
The oxidizing agent of the invention is preferably m-chloroperbenzoic acid ( m-CPBA ).
Treatment of ( VIII ) with m-chloroperbenzoic acid in dichloromethane ;.
Representative examples of the oxidizing agent are hydrogen peroxide, m-chloroperbenzoic acid, oxone and mixtures thereof.
