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  2. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    Benzylamine is used as a masked source of ammonia, since after N-alkylation, the benzyl group can be removed by hydrogenolysis: [10] C 6 H 5 CH 2 NH 2 + 2 RBr → C 6 H 5 CH 2 NR 2 + 2 HBr C 6 H 5 CH 2 NR 2 + H 2 → C 6 H 5 CH 3 + R 2 NH. Typically a base is employed in the first step to absorb the HBr (or related acid for other kinds of ...

  3. Schotten–Baumann reaction - Wikipedia

    en.wikipedia.org/wiki/Schotten–Baumann_reaction

    The name "Schotten–Baumann reaction conditions" often indicate the use of a two-phase solvent system, consisting of water and an organic solvent. The base within the water phase neutralizes the acid, generated in the reaction, while the starting materials and product remain in the organic phase, often dichloromethane or diethyl ether .

  4. Blanc chloromethylation - Wikipedia

    en.wikipedia.org/wiki/Blanc_chloromethylation

    The benzyl alcohol thus formed is quickly converted to the chloride under the reaction conditions. Mechanism of Blanc chloromethylation Other possibilities for the electrophile include (chloromethyl)oxonium cation (ClH 2 C–OH 2 + ) or chlorocarbenium cation (ClCH 2 + ), which may be formed in the presence of zinc chloride. [ 4 ]

  5. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl chloride, or α-chlorotoluene, is an organic compound with the formula C 6 H 5 CH 2 Cl. This colorless liquid is a reactive organochlorine compound that is a widely used chemical building block .

  6. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  7. Menshutkin reaction - Wikipedia

    en.wikipedia.org/wiki/Menshutkin_reaction

    As is typical for an S N 2 process, benzylic, allylic, and α-carbonylated alkyl halides are excellent reactants. Even though alkyl chlorides are poor alkylating agents ( gem -dichlorides especially so), amines should not be handled in chlorinated solvents such as dichloromethane and dichloroethane, especially at high temperatures, due to the ...

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  9. Diphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Diphenylmethane

    (c 6 h 5) 2 ch − + ch 3 ch 2 ch 2 ch 2 br → (c 6 h 5) 2 chch 2 ch 2 ch 2 ch 3 + br − Alkylation of various benzhydryl compounds has been demonstrated using the corresponding alkyl halides, both primary ( benzyl chloride , β-phenylethyl chloride , and n-octyl bromide) and secondary ( benzhydryl chloride , α-phenylethyl chloride , and ...