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HRID 1004793作成日:2026年10月25日

Aniline → 3-methoxy-N-phenylbenzamide

https://huagongshe.com/reaction/1004793

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物m-Anisoyl chlorideHCID 74374—
反応物3-Acetoxy-2-methylbenzoic acidHCID 3798557—
生成物3-methoxy-N-phenylbenzamideHCID 835330—

反応手順

WO 95/09843 describes a multistage process for the preparation of 3-acetoxy-2-methylbenzoic acid. This process starts from 3-methoxybenzoyl chloride. The 3-methoxybenzoyl chloride is reacted with aniline to give 3-methoxy-N-phenylbenzamide. In a second step, the 3-methoxy-N-phenylbenzamide is reacted with 2 equivalents of n-butyllithium and then alkylated using methyl iodide. 3-Methoxy-2-methyl-N-phenylbenzamide is formed here, which is then reacted with aqueous hydrochloric acid and aqueous hydrogen bromide in boiling acetic acid with hydrolysis of the amide group and cleavage of the methoxy group to give 3-hydroxy-2-methylbenzoic acid. The 3-hydroxy-2-methylbenzoic acid must be acylated with acetic anhydride in order to obtain the 3-acetoxy-2-methyl-benzoic acid. The individual reaction steps are described in greater detail in WO 95/09843 under Preparation 9 A, B and C and Example 81.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06051732
出典データセットuspto-grants-2000_04
ORD IDord-9e7fc6bf887443ad9f92b71527b3257d
出典メモuspto-grants-2000_04