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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21600생성일: 2026년 10월 24일

Chloromethyl ethyl ether → 1-ethoxymethyl-5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamide

https://huagongshe.com/ko/reaction/21600

반응식

참여 물질

역할이름HCID투입량
반응물Chloromethyl ethyl etherHCID 18523—
반응물Sodium hydrideHCID 24758—
반응물5-Methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamideHCID 10753063—
용매DimethylformamideHCID 6228—
용매HexaneHCID 8058—
생성물1-ethoxymethyl-5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamideHCID 1529453459.3%

반응 조건

온도0 °C

반응 단계

5-Methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamide (328 mg, 1.32 mmol) in 5 mL of dimethylformamide is added to a suspension of sodium hydride (60% by weight) (67 mg, 1.67 mol) in 5 mL of dimethylformamide. After 1.5 hours the mixture is cooled to 0° C. and chloromethyl ethyl ether (160 μL, 1.72 mmol) is added dropwise, and the solution is stirred at 0° C. for 20 minutes and then at room temperature for 1.5 hours. The reaction mixture is diluted with 1:1 hexane:ethyl acetate and washed with brine. The organic layer is dried over MgSO4, filtered, and concentrated in vacuo. Chromatography eluting with 1:1 ethyl acetate:hexane gives 240 mg (51%) of 1-ethoxymethyl-5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamide; mp 110°-112° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424329
출처 데이터셋uspto-grants-1995_06
ORD IDord-859a8129a115414292c81e086605f598
출처 메모uspto-grants-1995_06