4-benzylmorpholin-3-one-Morpholines| Ambeed

Chemistry Heterocyclic Building Blocks Morpholines 4-benzylmorpholin-3-one

4-benzylmorpholin-3-one

Ambeed provide 6 derivatives of 4-benzylmorpholin-3-one.

These compounds have the same murcko framework: 4-benzylmorpholin-3-one.

Reduction: The ketone group in 4-benzylmorpholin-3-one can be reduced to an alcohol using reducing agents like sodium borohydride (NaBH₄) or lithium aluminum hydride (LiAlH₄).
Acylation: The ketone group can undergo acylation reactions to form various derivatives. For example, it can react with acyl chlorides or anhydrides to form ketals or esters.
Nucleophilic Addition: The ketone carbon can undergo nucleophilic addition reactions, particularly if a strong nucleophile is present. This can lead to the formation of a new carbon-oxygen bond.
Grignard Reaction: 4-benzylmorpholin-3-one can react with a Grignard reagent (organomagnesium compound) to form a tertiary alcohol derivative.
Substitution Reactions: The benzyl group in 4-benzylmorpholin-3-one can potentially undergo substitution reactions, depending on the reaction conditions and the nature of the substituent.
Cyclization Reactions: Given the presence of the morpholine ring, intramolecular cyclization reactions might occur under appropriate conditions, leading to the formation of cyclic products.
Oxidation: The benzyl group can be oxidized to a carboxylic acid using strong oxidizing agents like potassium permanganate (KMnO₄) or chromic acid (H₂CrO₄).

4-benzylmorpholin-3-one

A127547106973-36-897%

$42.00/1g

A213353106973-37-997%

$46.00/1g

A166952287930-73-897%

$23.00/25g

A2505711235181-00-697%

$17.00/250mg

A15141261636-32-695%

$193.00/5g

A277879106910-81-097%

$111.00/5g