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HRID 356403作成日:2026年10月25日

Ethylamine → 3-Chloro-2-fluorobenzoic acid

https://huagongshe.com/reaction/356403

反応式

関与物質

役割名称HCID仕込み量
反応物EthylamineHCID 6341—
反応物3-Chloro-2-fluoro-6-(trimethylsilyl)benzoic acidHCID 18630211—
生成物3-Chloro-2-fluorobenzoic acidHCID 30293184%
生成物3-Chloro-N-ethyl-2-fluoro-6-(trimethylsilyl)benzamideHCID 18630098—

反応手順

The trimethylsilyl ester of 3-chloro-2-fluorobenzoic acid (11.66 g) was prepared in 84% yield using the method described in Example 207. This ester (2.47 g) was converted to 0.45 g of 3-chloro-2-fluoro-6-(trimethylsilyl)benzoic acid in 18% yield using the method of Example 207. The crude product was converted to the acid chloride by the procedure of example b. The acid chloride was reacted with 70% aq ethylamine using General Method E1 to afford the title compound. Purification by flash chromatography (ethyl acetate/hexanes) followed by recrystallization from pentane gave 84 mg of the title compound as an off-white solid (18%). m.p. 96°-97° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05834447
出典データセットuspto-grants-1998_11
ORD IDord-cbf7b3612c7c4f04ab141e5d8d612f1a
出典メモuspto-grants-1998_11