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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1847192생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1847192

반응식

참여 물질

역할이름HCID투입량
반응물Phenethyl bromideHCID 7666—
반응물Potassium CarbonateHCID 11430—
반응물6-Hydroxy-3,4-dihydro-1(2H)-naphthalenoneHCID 4679494—
용매AcetonitrileHCID 6342—
생성물6-(2-Phenylethoxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 1306733161.1%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08952151B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-43360678a19e486a907c35c5920027e4
출처 메모uspto-grants-2015_02