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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 992116생성일: 2026년 10월 23일

Water → Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-(methoxymethyloxy)-naphth-7-yl]naphth-2-oate

https://huagongshe.com/ko/reaction/992116

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Chloromethyl Methyl EtherHCID 7864—
반응물DiisopropylethylamineHCID 81531—
반응물Ethyl 6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-hydroxynaphth-2-yl]naphth-2-oateHCID 15462839—
반응물t-Butylammonium IodideHCID 22344722—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-(methoxymethyloxy)-naphth-7-yl]naphth-2-oateHCID 22571528—

반응 단계

To a cold (0° C.) solution of 130 mg (0.35 mmol) of ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-(hydroxy)-naphth-7-yl]naphth-2-oate (Compound B4) in 2.0 mL of methylene chloride was added 50 mg (0.15 mL, 0.86 mmol) of Hunig's base, followed by 0.21 g (0.20 mL, 2.6 mmol) chloromethyl methyl ether was added and stirred at room temperature for 14 h. About 500 mgs of t-butylammonium iodide was then added and the reaction was warmed to 35° C. for one additional hour. The reaction was diluted with water, and extracted with CH2Cl2 (2×). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. The title compound was obtained as an oil after flash chromatography (silica, 10% ethyl acetate).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06465663B2
출처 데이터셋uspto-grants-2002_10
ORD IDord-7decfbbd3e104bf9ad619b4a90d88a6d
출처 메모uspto-grants-2002_10