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HRID 30554作成日:2026年10月23日

Benzoyl chloride, 3-bromo- → 3-Bromo-N-methoxy-N-methylbenzamide

https://huagongshe.com/ja/reaction/30554

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chloride, 3-bromo-HCID 74377—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物DiisopropylethylamineHCID 81531—
溶媒DichloromethaneHCID 6344—
生成物3-Bromo-N-methoxy-N-methylbenzamideHCID 1216287590.3%

反応手順

A mixture of N-methoxymethanamine hydrochloride (22.1 g, 228.5 mmol), diisopropyl ethyl amine (63.5 mL, 365.6 mmol) and CH2Cl2 was treated dropwise with 3-bromobenzoyl chloride (15 g, 68.5 mmol) in CH2Cl2, stirred at room temperature for 30 minutes, and concentrated under vacuum. The resultant residue was dispersed in water and extracted with ethyl ether. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. The resultant residue was purified on silica gel (Biotage) using hexanes/EtOAc (2/1) as the eluting solvents to give 3-bromo-N-methoxy-N-methylbenzamide as a tan solid (15.1 g, 90% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423158B2
出典データセットuspto-grants-2008_09
ORD IDord-166da1d9e33a4bd8acda9bd0700ddbfe
出典メモuspto-grants-2008_09