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  2. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl ethers are often derived from benzyl chloride. Benzyl chloride reacts with aqueous sodium hydroxide to give dibenzyl ether . In organic synthesis , benzyl chloride is used to introduce the benzyl protecting group in reaction with alcohols , yielding the corresponding benzyl ether, carboxylic acids , and benzyl ester.

  3. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    The Williamson ether synthesis is an organic ... phasic system under phase transfer catalytic conditions is the reaction of benzyl chloride and furfuryl ...

  4. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.

  5. Menshutkin reaction - Wikipedia

    en.wikipedia.org/wiki/Menshutkin_reaction

    Some phase transfer catalysts (PTC) can be prepared according to the Menshutkin reaction, for instance the synthesis of triethyl benzyl ammonium chloride (TEBA) from triethylamine and benzyl chloride: Menshutkin reaction

  6. 4-Vinylbenzyl chloride - Wikipedia

    en.wikipedia.org/wiki/4-Vinylbenzyl_chloride

    4-Vinylbenzyl chloride is an organic compound with the formula ClCH 2 C 6 H 4 CH=CH 2. It is a bifunctional molecule, featuring both vinyl and a benzylic chloride functional groups . It is a colorless liquid that is typically stored with a stabilizer to suppress polymerization.

  7. Benzoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_chloride

    Benzoyl chloride, also known as benzenecarbonyl chloride, is an organochlorine compound with the formula C 7 H 5 ClO. It is a colourless, fuming liquid with an irritating odour, and consists of a benzene ring ( C 6 H 6 ) with an acyl chloride ( −C(=O)Cl ) substituent .

  8. Benzyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloroformate

    Benzyl chloroformate is commonly used in organic synthesis for the introduction of the benzyloxycarbonyl (formerly called carboxybenzyl) protecting group for amines.The protecting group is abbreviated Cbz or Z (in honor of discoverer Zervas), hence the alternative shorthand designation for benzyl chloroformate as Cbz-Cl or Z-Cl.

  9. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    Benzoic acid is cheap and readily available, so the laboratory synthesis of benzoic acid is mainly practiced for its pedagogical value. It is a common undergraduate preparation. Benzoic acid can be purified by recrystallization from water because of its high solubility in hot water and poor solubility in cold water.