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HRID 5376作成日:2026年10月23日

2-Chloroethyl methyl sulfide → 4-Amino-5-chloro-2-[2-(methylthio)ethoxy]benzoic acid

https://huagongshe.com/ja/reaction/5376

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloroethyl methyl sulfideHCID 10965—
反応物Sodium hydrideHCID 24758—
反応物4-Amino-5-chloro-2-hydroxybenzoic acidHCID 14883222—
溶媒DimethylformamideHCID 6228—
生成物4-Amino-5-chloro-2-[2-(methylthio)ethoxy]benzoic acidHCID 1910840557%

反応条件

温度25 °C

反応手順

A cooled (5° C.) suspension of 60% sodium hydride oil dispersion (0.52 g, 13 mmoles) in anhydrous dimethylformamide (15 mL) under nitrogen was treated in portions with 4-amino-5-chloro-2-hydroxybenzoic acid (0.94 g, 5 mmoles), stirred for 15 minutes at 25° C., treated with (2-chloroethyl)methyl sulfide (1.66 g, 15 mmoles), and heated to 100° C. for 18 hours. The solution is cooled, concentrated in vacuo, and added to water (25 mL). The aqueous solution is extracted with ether, and the extract is dried (MgSO4), concentrated in vacuo, taken up in 50% aqueous ethanol (50 mL), treated with potassium hydroxide (5.0 g), and refluxed for one hour. The mixture is concentrated, diluted with water to 75 mL total volume, extracted with ether, and acidified to pH 3 with concentrated HCl. The precipitate is filtered, washed with water, air dried, and recrystallized from ethyl acetate to afford 0.74 g (57%) of product as fine voluminous white needles, mp 137.5°-139.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244907
出典データセットuspto-grants-1993_09
ORD IDord-4a61892e548641678c1f2f77ac5daff8
出典メモuspto-grants-1993_09