戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1666301作成日:2026年10月27日

1,1'-Carbonyldiimidazole → N-(3-methoxy-benzyl)-N-methyl-2-(3,5-dichlorophenyl)-2-(phenylsulfanyl)-acetamide

https://huagongshe.com/reaction/1666301

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物3-Methoxy-N-methylbenzylamineHCID 5152225—
反応物2-(3,5-Dichlorophenyl)-2-(phenyl-sulfanyl)acetic acidHCID 67081802—
溶媒DichloromethaneHCID 6344—
生成物N-(3-methoxy-benzyl)-N-methyl-2-(3,5-dichlorophenyl)-2-(phenylsulfanyl)-acetamideHCID 6708195076.5%

反応手順

A solution of 2-(3,5-dichlorophenyl)-2-(phenyl-sulfanyl)acetic acid (1.65 g) in dichloromethane (50 ml) was treated with 1,1′-carbonyldiimidazole (0.90 g) at room temperature for 2 hours. A solution of N-methyl-3-methoxy-benzylamine (1.0 g) in dichloromethane (15 ml) was added and the stirring was continued for one hour. The reaction mixture was washed with aqueous hydrochloric acid (1M, 50 ml) and aqueous sodium hydroxide (1M, 50 ml). The organic phase was dried and concentrated to dryness leaving crude N-(3-methoxy-benzyl)-N-methyl-2-(3,5-dichlorophenyl)-2-(phenylsulfanyl)-acetamide (1.8 g) as a viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08044067B2
出典データセットuspto-grants-2011_10
ORD IDord-2bfcea556a594983b140437c4a5c38c2
出典メモuspto-grants-2011_10