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HRID 8200作成日:2026年10月24日

Boron trifluoride etherate → 4-(5-Oxo-tetrahydro-furan-3-yl)-benzoic Acid Ethyl Ester

https://huagongshe.com/ja/reaction/8200

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物4-(5-Methoxy-tetrahydro-furan-3-yl)-benzoic Acid Ethyl EsterHCID 69365300—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物4-(5-Oxo-tetrahydro-furan-3-yl)-benzoic Acid Ethyl EsterHCID 69363763—

反応手順

To a solution of 75% 3-chloroperbenzoic acid (2.7 g, 11.76 mmol) in dichloromethane (35 mL) is added magnesium sulfate (2.0 g, 16.6 mmol) and the mixture stirred for 30 min. Solids are removed by filtration and the filtrate treated with borontrifluoride etherate (0.5 mL, 3.92 mmol) and 4-(5-methoxy-tetrahydro-furan-3-yl)-benzoic acid ethyl ester (2.45 g, 9.8 mmol) in dichloromethane (5 mL). The mixture is stirred at room temperature 18 h, diluted with ether (200 mL) and washed with a 10% solution of sodium thiosulfite (150 mL), a saturated solution of sodium bicarbonate (150 mL) and brine. The mixture is dried over magnesium sulfate, filtered and concentrated in vacuo. The residue is chromatographed on SiO2 (elute with 20% ethyl acetate/hexanes) to yield the title compound, 2.2 g (96%), as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087626B2
出典データセットuspto-grants-2006_08
ORD IDord-533050e5611d4df3b3683b95512ad06a
出典メモuspto-grants-2006_08