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HRID 1614722作成日:2026年10月26日

4-Toluenesulfonyl chloride → 1-[(4-Methyl-phenyl)-sulfonyloxy]-3,4-dihydroxy benzene

https://huagongshe.com/reaction/1614722

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物Triethyl borateHCID 9009—
反応物1,2,4-BenzenetriolHCID 10787—
反応物Sodium hydrideHCID 24758—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物1-[(4-Methyl-phenyl)-sulfonyloxy]-3,4-dihydroxy benzeneHCID 1977252750.2%

反応手順

1.37 g of 1,2,4-trihydroxy benzene and 40 ml of anhydrous dimethylformamide were mixed together under an inert gas atmosphere and then 0.984 g of sodium hydride in suspension at 53% in oil were added slowly at 15°-20° C. The mixture was stirred for one hour and then 1.906 ml of triethyl borate were added, followed by stirring for one hour. Then, a solution of 2.072 g of tosyl chloride in 15 ml of dimethylformamide were added over 2 hours and the mixture was stirred for 4 hours at ambient temperature. The mixture was poured into a water-ice-hydrochloric acid mixture and extraction took place with ethyl acetate followed by evaporating to dryness. The crude residue was washed with petroleum ether and after chromatography on silica and eluting with a cyclohexane-ethyl acetate (1-1) mixture, 1.53 g of the expected product were obtained which was crystallized from a flugene-isopropyl ether mixture.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05198571
出典データセットuspto-grants-1993_03
ORD IDord-a930ef55b2d948f3a011b0fb40d92a05
出典メモuspto-grants-1993_03