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HRID 518943作成日:2026年10月27日

2-Naphthol → (2-(Naphthalen-2-yloxy)ethyl)acetamide

https://huagongshe.com/reaction/518943

反応式

関与物質

役割名称HCID仕込み量
反応物2-NaphtholHCID 8663—
反応物Ethyl AcetateHCID 8857—
反応物2-Methyl-2-oxazolineHCID 70713—
生成物(2-(Naphthalen-2-yloxy)ethyl)acetamideHCID 82041146—

反応条件

温度70 °C

反応手順

A 3-neck round bottom flask was charged with 2-methyl-2-oxazoline (5.9 mL, 69.4 mmol) followed by 2-naphthol (10.0 g, 69.4 mmol) at room temperature. The resulting mixture was heated to reflux and stirred for 6 h. Reaction was monitored by TLC analysis. Additional 2-methyl-2-oxazoline (2.5 mL, 29.4 mmol) was added to ensure complete conversion of the 2-naphthol and the reaction mixture was heated to reflux for 16 additional hours. The reaction mixture was cooled to 70° C. then poured into ethyl acetate (100 mL) and stirred for 15 min. The resulting slurry was filtered and washed with ethyl acetate (25 mL). The filter cake was further dried under vacuum to afford -(2-(naphthalen-2-yloxy)ethyl)acetamide as an off white solid (12.35 g, 77.7% yield). 1H NMR (DMSO-d6, 400 MHz) δ 8.179-8.126 (m, 1H), 8.84-7.79 (m, 3H), 7.7.48-7.43 (m, 1H), 7.37-7.32 (m, 2H), 7.18 (dd, j=2.59 Hz, 8.97 Hz, 1H) 4.11 (t, j=5.66, 2H), 3.48 (q, j=5.90 Hz, 2H), 1.85 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115237B2
出典データセットuspto-grants-2015_08
ORD IDord-bf38e48ca1c144df9fb40148915f6792
出典メモuspto-grants-2015_08