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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404322생성일: 2026년 10월 25일

Sodium hydride → 1-Cyclopropylidene-6-methoxy-2,3-dihydro-1H-indene

https://huagongshe.com/reaction/404322

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
반응물6-Methoxy-1-IndanoneHCID 334036—
반응물Cyclopropyltriphenylphosphonium bromideHCID 2723931—
용매TetrahydrofuranHCID 8028—
생성물1-Cyclopropylidene-6-methoxy-2,3-dihydro-1H-indeneHCID 5746758679%

반응 단계

NaH (1.5 g, 62 mmol) was added to a suspension of cyclopropyltriphenyl-phosphonium bromide (24 g, 62 mmol) (commercially available from Sigma-Aldrich, St. Louis, Mo., USA) in THF (100 mL), and the resulting mixture was stirred at room temperature for 2 hours. Then, 6-methoxy-1-indanone (H10.1) (Oakwood Products, Inc.) (5.00 g, 31 mmol) and tris(2-(2-methoxyethoxy)ethyl)amine (commercially available from Sigma-Aldrich, St. Louis, Mo., USA) (1.1 mL, 3.1 mmol) were added slowly. The resulting mixture was stirred at room temperature for 10 minutes and then at 62° C. for 4 hours. The reaction mixture was concentrated and purified by chromatography (silica gel, eluting with 1:9 EtOAc/hexane) to provide H10.2 (4.53 g, 79% yield) as a solid. MS ESI (pos.) M/E: 187.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748462B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-9ff4a501133b448da0eb5577c6dd38e4
출처 메모uspto-grants-2014_06