Home Chemistry Heterocyclic Building Blocks Pyrimidines 5-(Benzyloxy)Pyrimidine
Nucleophilic Substitution: The benzyl ether group (-C6H5CH2O-) can be cleaved by nucleophiles, such as strong acids or strong bases. This reaction can result in the formation of the corresponding hydroxy group or an alkylated product, depending on the reaction conditions.
Nucleophilic Addition: The pyrimidine ring can undergo nucleophilic addition reactions at various positions. For example, if a strong nucleophile attacks the C2 or C4 position of the pyrimidine ring, it can lead to the formation of substituted pyrimidine derivatives.
Acylation: The pyrimidine ring can undergo acylation reactions, where acyl groups (-CO-R) are added to the ring. This can be achieved using acylating agents and suitable reaction conditions.
Reduction: 5-(Benzyloxy)pyrimidine can be reduced to form the corresponding dihydro-5-(benzyloxy)pyrimidine using reducing agents like sodium borohydride (NaBH4).
N-alkylation: The nitrogen atoms in the pyrimidine ring can undergo alkylation reactions when treated with alkylating agents, resulting in the substitution of the hydrogen atom on the nitrogen.
Oxidation: The compound can undergo oxidation reactions under appropriate conditions to form oxidized derivatives.
Halogenation: 5-(Benzyloxy)pyrimidine can be halogenated at various positions on the pyrimidine ring using halogenating agents.
Condensation Reactions: It can participate in condensation reactions with other compounds containing suitable functional groups to form more complex molecules.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
5-(Benzyloxy)pyrimidine-2-carbonitrile
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :