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HRID 1069485作成日:2026年10月24日

Acetone → {[2-(7-Methoxy-benzo[1,3]dioxole-5-carbonyl)-benzenesulfonyl]-o-tolyl-amino}-acetic acid methyl ester

https://huagongshe.com/ja/reaction/1069485

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物IsopropanolHCID 3776—
反応物({2-[Hydroxy-(7-methoxy-benzo[1,3]dioxol-5-yl)-methyl]-benzenesulfonyl}-o-tolyl-amino)-acetic acid methyl esterHCID 22965597—
反応物Jones' reagentHCID 131709961—
溶媒Ethyl AcetateHCID 8857—
生成物{[2-(7-Methoxy-benzo[1,3]dioxole-5-carbonyl)-benzenesulfonyl]-o-tolyl-amino}-acetic acid methyl esterHCID 2296559659%

反応手順

To acetone (225 mL) was added ({2-[hydroxy-(7-methoxy-benzo[1,3]dioxol-5-yl)-methyl]-benzenesulfonyl}-o-tolyl-amino)-acetic acid methyl ester (4.17 g, 8.35 mmol), and 8N Jones reagent (4 mL). The mixture was stirred 15 minutes giving a suspended solid. Isopropanol (20 mL) was added followed by stirring for 15 minutes. The mixture was filtered, saturated sodium bicarbonate solution was added, and the solvent was removed in vacuo giving a paste. The paste was resuspended in ethyl acetate and water, filtered, and washed with saturated sodium bicarbonate, brine and dried over anhydrous magnesium sulfate. The solution was filtered and evaporated to a solid which was crystallized from ethyl acetate and ethyl ether giving a white solid, 2.41 g, 59% yield, mp 159-170° C. NMR spectra and elemental analysis were consistent with the structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06252070B1
出典データセットuspto-grants-2001_06
ORD IDord-8359ecf4f77845398f2050a98f4449de
出典メモuspto-grants-2001_06