戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 63085作成日:2026年10月25日

Phenethyl bromide → 6-(2-Phenylethoxy)-1,2,3,4-tetrahydronaphthalen-1-one

https://huagongshe.com/reaction/63085

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物Potassium CarbonateHCID 11430—
反応物6-Hydroxy-3,4-dihydro-1(2H)-naphthalenoneHCID 4679494—
溶媒AcetonitrileHCID 6342—
生成物6-(2-Phenylethoxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 1306733161.1%

反応手順

To a solution of 6-hydroxy-3,4-dihydro-1(2H)-naphthalenone (2.0 g, 12.3 mmol) and (2-bromoethyl)benzene (4.8 g, 25.8 mmol) in ACN (20 mL) was added potassium carbonate (3.4 g, 24.6 mmol) at rt. The solution was heated at reflux overnight. The reaction was filtered, concentrated, and purified by silica gel chromatography (PE/EtOAc/DCM=10:1:2) to give 2.0 g (61%) of the title compound as a brown oil. 1H NMR (300 MHz, CDCl3): δ 2.08-2.16 (2H, m), 2.62 (2H, t, J=6.3 Hz), 2.92 (2H, t, J=6.3 Hz), 3.13 (2H, t, J=7.2 Hz), 2.92 (2H, t, J=7.2 Hz), 6.71 (1H, d, J=2.1 Hz), 6.83 (1H, dd, J=2.4, 8.7 Hz), 7.27-7.38 (5H, m), 8.01 (1H, dd, J=8.7 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447045B2
出典データセットuspto-grants-2016_09
ORD IDord-af7c815808a2477ab142ff286c75a0cd
出典メモuspto-grants-2016_09