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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8200생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Boron trifluoride etherateHCID 8000—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물4-(5-Methoxy-tetrahydro-furan-3-yl)-benzoic Acid Ethyl EsterHCID 69365300—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물4-(5-Oxo-tetrahydro-furan-3-yl)-benzoic Acid Ethyl EsterHCID 69363763—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087626B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-533050e5611d4df3b3683b95512ad06a
출처 메모uspto-grants-2006_08