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Benzophenone imine is an organic compound with the formula of (C 6 H 5) 2 C=NH. A pale yellow liquid, benzophenone imine is used as a reagent in organic synthesis. [1]
Benzophenone is a naturally occurring organic compound with the formula (C 6 H 5) 2 CO, generally abbreviated Ph 2 CO. Benzophenone has been found in some fungi, fruits and plants, including grapes. [4] It is a white solid with a low melting point and rose-like odor [5] that is soluble in organic solvents. Benzophenone is the simplest ...
When R = H, the compound is a primary imine, when R is hydrocarbyl, the compound is a secondary imine. If this group is not a hydrogen atom, then the compound can sometimes be referred to as a Schiff base. [9] When R 3 is OH, the imine is called an oxime, and when R 3 is NH 2 the imine is called a hydrazone.
Benzophenone imine, an organic compound with the formula of (C 6 H 5) 2 C=NH 2-Aminofluorene , a synthetic arylamine Index of chemical compounds with the same molecular formula
Several strategies have been developed to overcome this based on reagents that serve as ammonia equivalents. The use of a benzophenone imine or silylamide can overcome this limitation, with subsequent hydrolysis furnishing the primary aniline. [37] [38] [39]
In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime.
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Many ketones contain the benzoyl group. They have the formula C 6 H 5 CO–R, an important example being benzophenone. Benzoyl esters and amides are common in organic chemistry. The esters are used as a protecting groups in organic synthesis, [4] which can be easily removed by hydrolysis in dilute basic solution.
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