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HRID 398246생성일: 2026년 10월 25일

Benzene → Ethyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetate

https://huagongshe.com/reaction/398246

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물IodineHCID 807—
반응물Ethyl bromoacetateHCID 7748—
반응물6-Methoxy-2-methyl-2,3-dihydro-1H-inden-1-oneHCID 231178—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
생성물Ethyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetateHCID 57181931—

반응 단계

A solution of 13.4 g of 6-methoxy-2-methylindanone and 21 g. of ethyl bromoacetate in 45 ml. benzene is added over a period of five minutes to 21 g. of zinc amalgam (prepared according to Org. Syn. Coll. Vol. 3) in 110 ml. benzene and 40 ml. dry ether. A few cyrstals of iodine are added to start the reaction, and the reaction mixture is maintained at reflux temperature (ca. 65°) with external heating. At three-hour intervals, two batches of 10 g. zinc amalgam and 10 g. bromoester are added and the mixture is then refluxed for 8 hours. After addition of 30 ml. of ethanol and 150 ml. of acetic acid, the mixture is poured into 700 ml. of 50% aqueous acetic acid. The organic layer is separated, and the aqueous layer is extracted twice with ether. The combined organic layers are washed thoroughly with water, ammonium hydroxide and water. Drying over sodium sulfate, evaporation of solvent in vacuo followed by pumping at 80° (bath temperature)(1-2 mm.) gives crude ethyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetate (ca. 18 g.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610854B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-5cc6b67c615a47e589140ab8fb740ff9
출처 메모uspto-grants-2003_08