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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1245427생성일: 2026년 10월 25일

Tetrahydrofuran → Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate

https://huagongshe.com/reaction/1245427

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
반응물Methyl 6-hydroxy-2-naphthoateHCID 390995—
용매DimethylformamideHCID 6228—
생성물Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylateHCID 1208548485%

반응 단계

3.3 g (83 mmol) of 60% sodium hydride in oil are added portionwise to a solution of 14 g (69 mmol) of methyl 6-hydroxynaphthalene-2-carboxylate in 180 ml of an equivolume mixture of tetrahydrofuran and dimethylformamide. After the evolution of gas has ceased, 8.7 ml (76 mmol) of methoxyethoxymethyl chloride are added dropwise. The reaction medium is stirred at room temperature for 3 hours, immersed into ice-cold water and extracted with ethyl ether. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 17 g of methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate are obtained in the form of a colorless oil, in a yield of 85%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07125869B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-561eae2879104e1584fc2cf404214913
출처 메모uspto-grants-2006_10