Synthetic Route of 3433-37-2, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 3433-37-2, Name is 2-(Hydroxymethyl)piperidine, molecular formula is C6H13NO. In a Article，once mentioned of 3433-37-2
(equation presented) The conjugate additions of beta- and gamma-chloroamines to acetylenic sulfones afford enamine sulfones, which then undergo intramolecular alkylation to produce the corresponding cyclic enamines. This provides a convenient route to substituted piperidines, indolizidines, quinolizidines, and pyrrolizidines. The enantioselective total synthesis of the alkaloid (-)-indolizidine 167B (also named gephyrotoxin 167B) was thus achieved by the cycloaddition of (S)-2-(2-chloroethyl)pyrrolidine to 1-(p-toluenesulfonyl)-1-pentyne, followed by stereoselective reduction of the enamine moiety and reductive desulfonylation.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Synthetic Route of 3433-37-2, you can also check out more blogs about3433-37-2
Reference：
Piperidine – Wikipedia,
Piperidine | C5H2931N – PubChem