Downstream synthetic route of 10338-57-5

As the paragraph descriping shows that 10338-57-5 is playing an increasingly important role.

10338-57-5, 4-(Piperidin-1-yl)benzaldehyde is a piperidines compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: To a solution of 2b (1.75 g, 10 mmol) and triethyl 4-phosphonocrotonate (3.3 mL, 15 mmol) in THF (40 mL), sodium hydride (60% dispersion in mineral oil, 800 mg, 20 mmol) was carefully added at 0 C under Ar. After the reaction mixture was stirred at ambient temperature for 3 h, the reaction was quenched by adding ethanol (1 mL) and water (20 mL), and the product was extracted with EtOAc (3 x 20 mL). The organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane/EtOAc [4:1]) to give 3b (1.9 g, 7.0 mmol, 70%) as yellow crystals., 10338-57-5

As the paragraph descriping shows that 10338-57-5 is playing an increasingly important role.

Reference:
Article; Kiyama, Masahiro; Iwano, Satoshi; Otsuka, Satoshi; Lu, Shijia W.; Obata, Rika; Miyawaki, Atsushi; Hirano, Takashi; Maki, Shojiro A.; Tetrahedron; vol. 74; 6; (2018); p. 652 – 660;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem