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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1876997생성일: 2026년 10월 25일

3-Heptanone → Ethyl 2-ethyl-5-(1-ethyl-1-hydroxypropyl)thiophene-3-carboxylate

https://huagongshe.com/reaction/1876997

반응식

참여 물질

역할이름HCID투입량
반응물3-HeptanoneHCID 7802—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 5-bromo-2-ethylthiophene-3-carboxylateHCID 68515411—
반응물HCID 178420663HCID 178420663—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-ethyl-5-(1-ethyl-1-hydroxypropyl)thiophene-3-carboxylateHCID 68512433—

반응 단계

To a solution of ethyl 5-bromo-2-ethylthiophene-3-carboxylate (3.00 g) synthesized in Example 69 (4) in tetrahydrofuran (50 mL) was added dropwise 1.0M isopropylmagnesium bromide-tetrahydrofuran solution (13.7 mL) at −45° C. After stirring under an argon atmosphere for 1 hr, 1.0M isopropylmagnesium bromide-tetrahydrofuran solution (13.7 mL) was added dropwise, and the mixture was stirred for 1 hr. 3-Heptanone (6.04 mL) was added dropwise, and the mixture was stirred at −45° C. for 1 hr, and at room temperature for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=3:17, volume ratio) to give the title compound (3.06 g, quantitative) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309580B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-888730f20d674d77a67762f5c23b3b4f
출처 메모uspto-grants-2012_11