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HRID 1587255作成日:2026年10月27日

Methanol → 4-n-Pentylcyclohexylmethyl 2,3-dicyano-4-hydroxyphenyl ether

https://huagongshe.com/reaction/1587255

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Potassium HydroxideHCID 14797—
反応物2,3-DicyanohydroquinoneHCID 78467—
反応物4-n-Pentylcyclohexylmethyl methanesulfonateHCID 54136698—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-n-Pentylcyclohexylmethyl 2,3-dicyano-4-hydroxyphenyl etherHCID 5716366031.5%

反応条件

温度50 °C

反応手順

5.6 g of 2,3-dicyanohydroquinone and 4.6 g of 85%-potassium hydroxide were added to a mixture solvent of 15 ml of methanol and 60 ml of N,N-dimethylformamide, followed by heating to 50° C. to provide a solution. To the solution, 11.0 g of 4-n-pentylcyclohexylmethyl methanesulfonate was added, followed by stirring for 3 hours at 100° C. After the reaction, the reaction mixture was poured into cold water and washed with ether. The water layer was acidified with 6N-hydrochloric acid aqueous solution until a pH value of 1 was shown, and was subjected to extraction with ether. The organic layer was washed successively with 5%-sodium hydrogenecarbonate aqueous solution and water, followed by drying with anhydrous magnesium sulfate and distilling-off of the solvent to obtain a crude product. The crude product was purified by silica gel column chromatography (eluent: toluene/ethyl acetate) and treated with activated carbon, followed by recrystallization from methanol to obtain 3.6 g of 4-n-pentylcyclohexylmethyl 2,3-dicyano- 4-hydroxyphenyl ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05217643
出典データセットuspto-grants-1993_06
ORD IDord-ee7b48c448ea454e9defaadd2c008c0d
出典メモuspto-grants-1993_06