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HRID 1677342作成日:2026年10月25日

Acetone → 2-Bromo-1-thiophen-3-yl-butan-1-one

https://huagongshe.com/reaction/1677342

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物tert-ButanolHCID 6386—
反応物2-Bromo-1-thiophen-3-yl-butan-1-oneHCID 59598618—
反応物HCID 178461630HCID 178461630—
溶媒BenzeneHCID 241—
生成物2-Bromo-1-thiophen-3-yl-butan-1-oneHCID 59598618—
生成物5-Thiophen-3-yl-heptane-2,4-dioneHCID 59598638—

反応条件

温度0 °C

反応手順

EtMgBr (6.69 ml, 13 mmol, 2 M in ethyl ether) in benzene (10 ml) was cooled to zero degrees C., and tBuOH (1.28 ml, 13 mmol) was slowly added. The reaction mixture was stirred at zero degrees C. for 5 minutes, then acetone (530 ul, 7 mmol) was added, followed by a solution of 2-Bromo-1-thiophen-3-yl-butan-1-one (1.3 g, 6 mmol) in 3 ml benzene via cannula. The reaction mixture was heated to reflux for 1 hour, and acetone (250 ul) was added. The reaction mixture was heated 2 hours more at reflux. The reaction was cooled, quenched with 1 N HCl (10 ml), extracted three times with diethyl ether, washed brine, and dried over magnesium sulfate. The solvent was removed in vacuo and the residue chromatographed (5% ethyl acetate/hexanes) to give 247 mg of 2-Bromo-1-thiophen-3-yl-butan-1-one starting material and 520 mg of 5-Thiophen-3-yl-heptane-2,4-dione, 44%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08008313B2
出典データセットuspto-grants-2011_08
ORD IDord-2bc1373aa4cf4991a1cbb14e81d7f24a
出典メモuspto-grants-2011_08