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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1265279생성일: 2026년 10월 27일

Sodium hydride → 2-(Naphthalene-1-carbonyl)4-oxo-4-phenyl-butyric acid ethyl ester

https://huagongshe.com/reaction/1265279

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ethyl 3-(naphthalen-8-yl)-3-oxopropanoateHCID 2760157—
용매TolueneHCID 1140—
생성물2-(Naphthalene-1-carbonyl)4-oxo-4-phenyl-butyric acid ethyl esterHCID 2058275199.4%

반응 단계

A suspension of NaH (60% in mineral oil, 323 mg, 8.07 mmol) in toluene (20 mL) was treated with 3-Naphthalen-1-yl-3-oxo-propionic acid ethyl ester (1.63 g, 6.7 mmol). The resulting suspension was stirred at rt under Ar for 1 h, then treated with 2-bromocetophenone (1.61 g, 8.07 mmol). The suspension was immersed in a 70° C. oil bath and stirred under Ar for 4 h, cooled to rt, diluted with toluene and washed with H2O and brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified via flash chromatography (SiO2, 10-20% EtOAc/Heptane) to afford 2-(Naphthalene-1-carbonyl)-4-oxo-4-phenyl-butyric acid ethyl ester (1.2 g) contaminated with a small amount of unidentified aromatic impurity: 11H NMR (CDCl3, chemical shifts in ppm relative to TMS): 1.03 (t, 3H, J=7.25 Hz), 3.72 (dd, 1H, J=18.8 Hz, J=5.4 Hz), 3.96 (dd, 1H, J=18.8 Hz, J=8.05 Hz), 4.09 (m, 2H), 5.16 (m, 1H), 7.45-7.63 (m, 6H), 7.88 (d, 1H, J=7.9 Hz), 8.0-8.07 (m, 3H), 8.24 (d, 1H, J=7.2 Hz)), 8,48 (d, 1H, J=8.7 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06545108B1
출처 데이터셋uspto-grants-2003_04
ORD IDord-da59cb7ec6fb47959699c69dc3e3fc1d
출처 메모uspto-grants-2003_04