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HRID 168作成日:2026年10月24日

1-Chloro-4-(trifluoromethyl)benzene → Methyl 2-methyl-2-[4-(trifluoromethyl)anilino]propanoate

https://huagongshe.com/ja/reaction/168

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-4-(trifluoromethyl)benzeneHCID 7394—
反応物Methyl 2-amino-2-methylpropanoateHCID 4186341—
試薬Sodium t-butoxideHCID 23676156—
触媒Palladium (II) acetateHCID 4144353—
触媒Bis(adamantan-1-yl)(butyl)phosphaneHCID 11371790—
溶媒(Trifluoromethyl)benzeneHCID 7368—
生成物Methyl 2-methyl-2-[4-(trifluoromethyl)anilino]propanoateHCID 1175597940%

反応条件

温度180 °C

反応手順

1-chloro-4-(trifluoromethyl)benzene (0.068 mL, 0.51 mmol), methyl 2-amino-2-methylpropanoate (0.05 g, 0.43 mmol),BUTYLDI-1-ADAMANTYLPHOSPHINE (0.015 g, 0.04 mmol), sodium 2-methylpropan-2-olate (0.082 g, 0.85 mmol) and diacetoxypalladium (4.79 mg, 0.02 mmol) was added to a microwave vial. (TRIFLUOROMETHYL)-BENZENE (0.5 mL) was used as solvent, before use the solvent was bubbled with nitrogen (1-1.2 mL/mmol amine). The mixture was bubbled with nitrogen before the vial was sealed. The mixture was heated in microwave at 180° for 60min.. The mixture was heated in microwave at 180° for 60min. No conversion of startingmaterial was observed.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-d712f5c0551541748b4f06a98eb63af5
出典メモ750 AstraZeneca ELN dataset