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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2275192생성일: 2026년 10월 25일

Bis(2-bromoethyl) ether → 7-Methoxy-2',3,3',4,5',6'-hexahydro-2H-spiro [naphthalene-1,4'-pyran]-2-one

https://huagongshe.com/reaction/2275192

반응식

참여 물질

역할이름HCID투입량
반응물Bis(2-bromoethyl) etherHCID 21521—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물7-Methoxy-2-tetraloneHCID 77785—
용매TetrahydrofuranHCID 8028—
생성물7-Methoxy-2',3,3',4,5',6'-hexahydro-2H-spiro [naphthalene-1,4'-pyran]-2-oneHCID 6683398751%

반응 단계

To the THF (300 ml) solution of 7-methoxy-3,4-dihydro-1H-naphthalen-2-one (Compound A1, 20 g, 0.11 mol), sodium hydride (9.9 g, 3.7 eq.) was added at 0° C. After stirring for 10 min, 1-bromo-2-(2-bromo-ethoxy)-ethane (19 ml, 12 eq.) was added dropwise thereto, and the mixture was stirred at 80° C. for 3 hr. To the reaction solution, saturated aqueous solution of ammonium chloride was added and the extraction was carried out twice with ethyl acetate. The organic layer was dried over magnesium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (white solid, 13 g, 51%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09126931B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-392aa1cb81394130ba2ee0a3db6cced4
출처 메모uspto-grants-2015_09