돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1072107생성일: 2026년 10월 26일

Sodium hydride → Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate

https://huagongshe.com/reaction/1072107

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
반응물Methyl 6-hydroxy-2-naphthoateHCID 390995—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylateHCID 12085484—

반응 단계

14 g (69 mmol) of methyl 6-hydroxynaph-thalene-2-carboxylate in 90 ml of dimethylformamide and 90 ml of tetrahydrofuran are introduced into a round-bottomed flask and under a nitrogen stream. 3.3 g (82 mmol) of sodium hydride at 60% are added in small portions. When the gas emission has ceased, 8.7 ml (76 mmol) of 2-methoxyethoxymethyl chloride are added and the reaction medium is stirred for 3 hours at room temperature. It is then poured into ice-cold water and extracted with ether. The organic phase is dried over magnesium sulphate, filtered and evaporated off. The residue obtained is purified by chromatography on a silica column eluted with a heptane and ethyl acetate (80/20) mixture and 17 g (85%) of the expected product are obtained in the form of a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06908939B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-eb23a3d8fea94d1780e4a9ebee2e96e5
출처 메모uspto-grants-2005_06