戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 444444作成日:2026年10月25日

Solketal → 3-[(3-Methoxypyridin-2-yl)oxy]propane-1,2-diol

https://huagongshe.com/reaction/444444

反応式

関与物質

役割名称HCID仕込み量
反応物SolketalHCID 7528—
反応物Sodium hydrideHCID 24758—
反応物3-Methoxy-2-nitropyridineHCID 556063—
溶媒HexamethylphosphoramideHCID 12679—
生成物3-[(3-Methoxypyridin-2-yl)oxy]propane-1,2-diolHCID 13195074—

反応手順

26.5 g of sodium hydride are added in the course of one hour to a mixture of 161 g of 3-methoxy-2-nitropyridine and 144 g of 2,2-dimethyl-5-hydroxymethyl-1,3-dioxolane in 1,000 ml of hexamethylphosphoric acid triamide, with stirring; by means of cooling, the temperature is kept at 0°-10° during the addition. The reaction mixture is then stirred for a further 5 hours with ice-cooling and then for 15 hours at room temperature. The reaction mixture is poured onto ice and extracted with diethyl ether. The organic extract is washed with a concentrated aqueous solution of sodium chloride, dried and evaporated. The residue is dissolved in 1,000 ml of ethanol, 100 ml of 2 N hydrochloric acid are added and the mixture is left to stand for 8 hours. After evaporating off the solvent, the residue is rendered alkaline with a concentrated solution of sodium hydroxide in water and extracted with ethyl acetate. Evaporating off the solvent yields a crude product from which crystalline 3-(3-methoxy-2-pyridyloxy)-1,2-propanediol with a melting point of 62°-65° is obtained on the addition of diethyl ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04264599
出典データセットuspto-grants-1981_04
ORD IDord-cb9ffa13d32d4036b5c5f24a2f2a61e9
出典メモuspto-grants-1981_04