戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2110035作成日:2026年10月27日

Acetic Acid → 2-Amino-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/2110035

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物TriethylamineHCID 8471—
反応物Benzoic acid, 2-amino-5-iodo-HCID 72911—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物HCID 178418416HCID 178418416—
触媒palladium(II) acetateHCID 167845—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-Amino-5-(methoxycarbonyl)benzoic acidHCID 13105036—

反応条件

温度80 °C

反応手順

After dissolving 2-amino-5-iodobenzoic acid (4 mmol, 1052 mg) in DMF (10 ml) and MeOH (5 ml), NEt3 (3 eq, 1.67 ml) was added. Next, palladium acetate (0.1 eq, 90 mg) and dppp (0.1 eq, 165 mg) were added, carbon monoxide substitution was carried out, and the mixture was stirred at 80° C. for 5 hours. Upon completion of the reaction, acetic acid (2.5 ml) was added to suspend the reaction. Water (50 ml) was added, and extraction was performed with ethyl acetate (50 ml×3 times). The organic layer was washed with water (100 ml×2 times) and then dried over sodium sulfate. After concentration, a developing solvent (Hex/AcOEt=4/1→1/1) was used for purification by silica gel chromatography to obtain 2-amino-5-(methoxycarbonyl)benzoic acid. The compound was identified by LC-MS.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07517875B2
出典データセットuspto-grants-2009_04
ORD IDord-048688c5d3694dddb090ba85c4bb8d4f
出典メモuspto-grants-2009_04