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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63089생성일: 2026년 10월 25일

Triphenylphosphine → 6-(2-Cyclopropylethoxy)-1,2,3,4-tetrahydronaphthalen-1-one

https://huagongshe.com/reaction/63089

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2-Cyclopropylethan-1-olHCID 137642—
반응물6-Hydroxy-3,4-dihydro-1(2H)-naphthalenoneHCID 4679494—
반응물Diethyl azodicarboxylateHCID 5462977—
용매TetrahydrofuranHCID 8028—
생성물6-(2-Cyclopropylethoxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 6559909834%

반응 단계

To a suspension of 6-hydroxy-3,4-dihydro-1(2H)-naphthalenone (1.0 g, 6.0 mmol), 2-cyclopropylethanol (640 mg, 7.0 mmol) and triphenylphosphine (3.25 g, 12 mmol) in THF (100 mL) was added DEAD (2.13 g, 12 mmol) at 0° C. The reaction was stirred at rt overnight. The solution was concentrated and purified by silica gel chromatography (PE:EtOAc=12:1) to give 470 mg (33%) of the title compound as a red oil. 1H NMR (300 MHz, CDCl3): δ 0.13-0.15 (2H, m), 0.50-0.52 (2H, m), 0.86-0.93 (1H, m), 1.68-1.74 (2H, m), 2.11-2.15 (2H, m), 2.64 (2H, t, J=6.3 Hz), 2.93 (2H, t, J=6.0 Hz), 4.10 (2H, t, J=6.6 Hz), 6.73 (1H, s), 6.83 (1H, dd, J=2.4, 8.7 Hz), 8.02 (1H, d, J=8.7 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447045B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-e0b78794a7114837b8a773ee7e78cf55
출처 메모uspto-grants-2016_09