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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 618753생성일: 2026년 10월 24일

Sodium hydride → Ethyl 5-benzyloxy-1-(2-chloro-4,5-methylenedioxybenzyl)indole-2-carboxylate

https://huagongshe.com/ko/reaction/618753

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물6-Chloropiperonyl chlorideHCID 90113—
반응물Ethyl 5-(phenylmethoxy)-1H-indole-2-carboxylateHCID 95721—
용매DimethylformamideHCID 6228—
생성물Ethyl 5-benzyloxy-1-(2-chloro-4,5-methylenedioxybenzyl)indole-2-carboxylateHCID 1543318950%

반응 단계

To a stirring suspension of sodium hydride (2.03grams (hereinafter "g"), (60% in mineral oil), 50.8 millimoles (hereinafter "mmol")) in DMF (100 milliliters (hereinafter "mL")) was added ethyl 5-benzyloxyindole-2-carboxylate (10.0 g, 33.9 mmol). After 10 minutes (hereinafter "min"), 6-chloropiperonyl chloride (10.4 g, 50.8 mmol) was added. After 1 hour, the mixture was partitioned between water and ethyl acetate. The organic layer was washed with water and saturated brine, dried (MgSO4), filtered and concentrated to leave an oily pale yellow solid. The solid was recrystallized from ethanol to provide the title compound as a white solid (7.8 g, 50%). 1HNMR (400 MHz, CDCl3) d 7.49-7.33 (m, 6H), 7.19-7.08 (m, 3H), 6.87 (s, 1H), 5.86 (s, 2H), 5.78 (s, 1H), 5.77 (s, 2H), 5.11 (s, 2H), 4.33 (q, 2H), 1.36 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05955492
출처 데이터셋uspto-grants-1999_09
ORD IDord-2a19717096534eaabe645841464d90bb
출처 메모uspto-grants-1999_09