戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 719181作成日:2026年10月25日

Methyl iodide → 8-Amino-2-naphthalenol

https://huagongshe.com/reaction/719181

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物8-Amino-2-naphthalenolHCID 8358—
反応物Cleve's acidHCID 8386—
反応物Sodium hydrideHCID 24758—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物8-Amino-2-naphthalenolHCID 8358—
生成物7-Methoxynaphthalen-1-amineHCID 235817—

反応手順

8-Amino-naphthalen-2-ol was prepared from 8-amino-2-naphthalenesulphonic acid (commercially available) according to the literature (J. Org. Chem. 1949, p351). To a solution of 8-amino-naphthalen-2-ol (8.00 g) in dry N,N-dimethylformamide (80 mL) was added sodium hydride (60% dispersion in mineral oil, 3.2 g) carefully. After stirring for 4 hours the reaction mixture was cooled in an ice bath and methyl iodide (3.13 mL) was added dropwise. The reaction mixture was then stirred at room temperature for 3 days. Water (10 mL) was then added and the volatiles were removed in vacuo. The residue was dissolved in chloroform, washed with water, dried (MgSO4) and the solvent removed in vacuo to yield a dark oil. This was purified using flash chromatography (chloroform) to yield 7-methoxy-naphthalen-1-ylamine as a dark brown liquid (2.92 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07132419B2
出典データセットuspto-grants-2006_11
ORD IDord-d39c13159e5342e598803700f91173f1
出典メモuspto-grants-2006_11