Category: 939-23-1

Electric Literature of 939-23-1, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 939-23-1, name is 4-Phenylpyridine. This compound has unique chemical properties. The synthetic route is as follows.

EXAMPLE 90 4-Phenylpyridine (15.5 g., 0.1 mole) dissolved in 185 ml. of absolute ethanol and 15 ml. of concentrated hydrochloric acid was reduced with hydrogen over 2 g. of platinum oxide under a hydrogen pressure of about 55 pounds p.s.i.g. The product was worked up in the manner described above in Example 72 and isolated in the form of the hydrochloride salt to give 15.3 g. of 4-cyclohexylpiperidine hydrochloride. (The free base gives m.p. 106-109 C.)

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 939-23-1, 4-Phenylpyridine.

Reference:
Patent; Sterling Drug Inc.; US4160862; (1979); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

In the chemical reaction process,reaction time,type of solvent,can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product.An updated downstream synthesis route of 939-23-1 as follows., 939-23-1

To a solution of 4-phenylpyridine (15.5 g, 0.1 mol) in acetone (100 mL) was added 1,3-propane sultone (12.2 g, 0.1 mol) at room temperature. The mixture was then heated at reflux temperature overnight. The resultant suspension was cooled to room temperature. The solid was collected by filtration and washed with acetone. To a solution of the solid (31 g) in methanol (500 mL) was added sodium borohydride (10 g, 260 mmol) portionwise, and the mixture was stirred at room temperature for 2 h. Distilled water (50 mL) was added to destroy the excess of sodium borohydride. The mixture was diluted with methanol (200 mL), and neutralized with Amberlite IR-120 ion-exchange resin (H+ form, 300 g). A white precipitate was formed. The precipitate and the resin were removed by filtration and treated with distilled water (400 mL) at 100 C. The mixture was filtered and the residual resin was washed with hot distilled water (2¡Á200 mL). The filtrates and washings were combined and concentrated to dryness. The residue was co-evaporated with methanol (3¡Á200 mL), and then recrystallized from ethanol-water {8:2 (v/v)} to afford 4-phenyl-1-(3′-sulfopropyl)-1,2,3,6-tetrahydropyridine as white crystals (26 g, 93%). The 1H and 13C NMR spectra were in agreement with the structure.

The chemical industry reduces the impact on the environment during synthesis 939-23-1, I believe this compound will play a more active role in future production and life.

Reference:
Patent; Neurochem (International) Limited; Isis Innovation Limited; Queen’s University at Kingston; The University of British Columbia; The Governing Counsel of The University of Toronto; US2007/15737; (2007); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem