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HRID 398246作成日:2026年10月26日

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

https://huagongshe.com/reaction/398246

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物IodineHCID 807—
反応物Ethyl bromoacetateHCID 7748—
反応物6-Methoxy-2-methyl-2,3-dihydro-1H-inden-1-oneHCID 231178—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetateHCID 57181931—

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610854B2
出典データセットuspto-grants-2003_08
ORD IDord-5cc6b67c615a47e589140ab8fb740ff9
出典メモuspto-grants-2003_08