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HRID 1430761作成日:2026年10月25日

2,5-Dimethylfuran → (1RS,2SR,6RS,7SR)-4-(5-bromo-2-ethylphenyl)-1,7-dimethyl-10-oxatricyclo[5.2.1.02,6]dec-8-en-3,5-dione

https://huagongshe.com/reaction/1430761

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-DimethylfuranHCID 12266—
反応物Magnesium diiodideHCID 5462737—
反応物2-(5-Bromo-2-ethylphenyl)cyclopent-4-ene-1,3-dioneHCID 58061486—
溶媒DichloromethaneHCID 6344—
生成物(1RS,2SR,6RS,7SR)-4-(5-bromo-2-ethylphenyl)-1,7-dimethyl-10-oxatricyclo[5.2.1.02,6]dec-8-en-3,5-dioneHCID 67284135—

反応手順

2,5-Dimethylfuran (2.3 ml, 21.6 mmol) and magnesium iodide (0.40 g, 1.4 mmol) are added to a solution of 2-(5-bromo-2-ethylphenyl)cyclopent-4-ene-1,3-dione (2.0 g, 7.2 mmol) in dichloromethane (10 ml) and the mixture is stirred at room temperature for 3 days. The reaction mixture is concentrated under reduced pressure and the residue is purified by column chromatography on silica gel to give (1RS,2SR,6RS,7SR)-4-(5-bromo-2-ethylphenyl)-1,7-dimethyl-10-oxatricyclo[5.2.1.02,6]dec-8-en-3,5-dione.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08940913B2
出典データセットuspto-grants-2015_01
ORD IDord-0bb9ee0336ec4614886ec8399a00418f
出典メモuspto-grants-2015_01