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HRID 1653627作成日:2026年10月25日

Acetic Acid → 2-Isopropylthio-3-(cyclohexanon-2-yloxy)-pyridine

https://huagongshe.com/reaction/1653627

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Potassium CarbonateHCID 11430—
反応物2-ChlorocyclohexanoneHCID 13203—
反応物3-Pyridinol, 2-[(1-methylethyl)thio]-HCID 19957932—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2-Isopropylthio-3-(cyclohexanon-2-yloxy)-pyridineHCID 5701835572.7%

反応手順

7.29 g of 2-chlorocyclohexanone are added at room temperature to a mixture of 8.4 g of 2-isopropylthio-3-hydroxypyridine and 7.6 g of potassium carbonate in 120 ml of dimethylformamide, and the mixture is stirred for one hour at 45°-50° C. After the addition of 1.46 g of 2-chlorocyclohexanone and 1.52 g of potassium carbonate and after 2 hours of a further analogous addition of 0.73 g of 2-chlorocyclohexanone and 0.76 g of potassium carbonate, the suspension is stirred for a further 3.5 hours at 45°-50° C. The resulting reaction solution is poured onto a mixture consisting of 200 ml of ice-water, 50 ml of 2N acetic acid and 100 ml of ethyl acetate, washed three times with 300 ml of ethyl acetate and 100 ml of saturated sodium chloride solution each time, dried over sodium sulfate and concentrated by evaporation. The residue is triturated with petroleum ether and filtered. 9.57 g of the desired ketone having a melting point of 106°-110° C. are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05403814
出典データセットuspto-grants-1995_04
ORD IDord-46014526f7844a69a3bd3795aa33ee8d
出典メモuspto-grants-1995_04