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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38426생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/38426

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물tert-ButanolHCID 6386—
반응물2-Bromo-1-thiophen-3-yl-butan-1-oneHCID 59598618—
반응물HCID 178461630HCID 178461630—
용매BenzeneHCID 241—
생성물2-Bromo-1-thiophen-3-yl-butan-1-oneHCID 59598618—
생성물5-Thiophen-3-yl-heptane-2,4-dioneHCID 59598638—

반응 조건

온도0 °C

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524725B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-bc19b9a175a54cfebeeaa16f982df689
출처 메모uspto-grants-2013_09