6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Related Products of 1122-71-0
Syntheses of methylpyridine derivatives. VI. Reaction of 2,6-lutidine 1-oxide with phosphoryl chloride was written by Kato, Tetsuzo. And the article was included in Yakugaku Zasshi in 1955.Related Products of 1122-71-0 This article mentions the following:
2,6-Me2C5H3N → O.HCl (8 g.) and 23 g. POCl3 heated 20 min. at 100°, 30 min. at 120-30°, and 4 hrs. at 145-50% the POCl3 removed in vacuo, the residue poured into 150 ml. ice water, made alk. with Na2CO3 and extracted with Et2O gave 6 g. product, fractionation of which yielded 4.5 g. composed mainly of 4,2,6-ClMe2C5H2N, b90 108-13° (picrate, m. 166-7°; HCl salt, m.p. above 260°), and a small amount of 6,2-Me(ClCH2) C5H3N (XV); XV.picrate, m. 162-4°. XV (5 g.), b65 118-20°, in 50 ml. PhMe and 4.7 g. PhCH2CN at 0° treated portionwise with 2.8 g. NaNH2, heated 1 hr. at 100-10°, the product poured into ice water, extracted with C6H6 and distilled to give 4 g. R2CH2CHPhCN (XVI, R2 = 6-methyl-2-pyridyl), b3 163-9°; XVI.H2O, m. 52-60°; XVI picrate, m. 156-8°. XVI (2 g.) treated with 8 ml. 98% H2SO4 with cooling, let stand 1 day, the product poured into 50 ml. ice water, neutralized with Na2CO3, extracted with CHCl3 and Et2O added to give 1.4 g. R2CH2CHPhCONH2 (XVII), plates, m. 158° (from Me2CO). XVII (2 g.) in 30 ml. EtOH refluxed 4 hrs. while passing in dry HCl gas (XVIII), the NH4Cl and EtOH removed, the residue neutralized with Na2CO3 and extracted with Et2O gave 1.4 g. R2CH2CHPhCO2Et (XIX), b2 140-2°. XIX (0.7 g.) and 5 ml. 10% HCl refluxed 30 min., the product concentrated in vacuo, neutralized with Na2CO3 and extd with Me2CO gave 0.2 g. R2CH2CHPhCO2H (XX), needles, m. 105-15°. XX (0.5 g.) in 1 ml. 15% K2CO3 heated on a water bath, the product mixed with 1 g. Ca(OH)2 and dry distilled to give 0.5 g. 6,2-Me(PhCH2CH2)C5H3N, b12 155-8°; picrate, m. 118-19°. 6,2-Me(HOCH2)C5H3N (1.2 g.) in 10 ml. CHCl3 treated dropwise with 1.3 g. SOCl2 in 10 ml. CHCl3, refluxed 30 min., the solvent and SOCl2 removed and the residue recrystallized from Me2CO gave 1.4 g. XV.HCl, m. 146-53°; XV picrate, m. 163-4°. In the experiment, the researchers used many compounds, for example, 6-Methyl-2-pyridinemethanol (cas: 1122-71-0Related Products of 1122-71-0).
6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Related Products of 1122-71-0
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts