戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 31739作成日:2026年10月23日

Trifluoroacetic acid → 4-acetyl-N-(3-methoxybenzyl)benzamide

https://huagongshe.com/ja/reaction/31739

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物4-MethylmorpholineHCID 7972—
反応物4-Acetylbenzoic AcidHCID 11470—
反応物3-MethoxybenzylamineHCID 21156—
反応物PyBOPHCID 2724699—
溶媒DichloromethaneHCID 6344—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物4-acetyl-N-(3-methoxybenzyl)benzamideHCID 5984089597%

反応手順

The Sasrin resin was prepared as described in Step 2 of Example 3. The resin (500 mg) was heated with a solution of 3-methoxybenzylamine (600 μl ) in NMP (6 ml) at 70° C. for 4 hours. The resin was then washed with DMF and dichloromethane and then shaken with a solution of PyBop® (1.04 g, 2 mmol), 4-acetylbenzoic acid (0.33 g, 2 mmol), 4-methylmorpholine (4 mmol) in NMP (6 ml) at room temperature overnight. A small aliquot of the resin was treated with 20% TFA in dichloromethane to give the intermediate, (4-acetylphenyl)-N-[(3-methoxyphenyl)methyl]carboxamide (HPLC: 23.94 min (97%); MS; MH+=284 (as required)). The resin was then heated at 95° C. for 7 hours in DMFDMA (5 ml).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425557B2
出典データセットuspto-grants-2008_09
ORD IDord-1818aeeacb4c4b8996cc79a60014620c
出典メモuspto-grants-2008_09