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HRID 2334作成日:2026年10月23日

Thionyl Chloride → Methyl 3-(4-pentenoylamino)benzoate

https://huagongshe.com/ja/reaction/2334

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物4-Pentenoic acidHCID 61138—
反応物Benzoic acid, 3-amino-, methyl esterHCID 78274—
反応物4-Pentenoyl chlorideHCID 4228493—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物Methyl 3-(4-pentenoylamino)benzoateHCID 1077599432%

反応手順

Methyl(3-amino)benzoate (4.5 g, 29.8 mmol) was taken up in DCM (10 ml) and pyridine (1 ml) at 0° C. 4-Pentenoyl chloride (freshly prepared from 4-pentenoic acid (3.0 g, 29.97 mmol) and thionyl chloride (6.6 ml) at r.t. for 1 h, evaporated and azeotroped with DCM) was added dropwise in DCM (3 ml). The mixture was allowed to warm to r.t. and stirred overnight. The mixture was evaporated and partitioned between EtOAc and 1M HCl. The organic portion was washed with 5% KHCO3 and brine, filtered (Whatman® 1PS, phase separator), and evaporated. The residue was chromatographed (eluant 30% EtOAc in hexanes) to provide a colourless oil (2.20 g, 32%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728829
出典データセットuspto-grants-1998_03
ORD IDord-21d973d5e9c342b28599ca4532af6af7
出典メモuspto-grants-1998_03