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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2221642생성일: 2026년 10월 26일

2-Oxime 2,3-butanedione → Ethyl 5-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)thiophene-2-carboxylate

https://huagongshe.com/reaction/2221642

반응식

참여 물질

역할이름HCID투입량
반응물2-Oxime 2,3-butanedioneHCID 6398969—
반응물Ethyl 5-formylthiophene-2-carboxylateHCID 10797570—
반응물Hydrogen chloride-ethyl acetateHCID 21866389—
생성물Ethyl 5-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)thiophene-2-carboxylateHCID 2307661424%

반응 단계

A mixture of ethyl 5-formylthiophene-2-carboxylate (14.6 g), 2,3-butanedione-2-oxime (8.02 g) and 4N hydrogenchloride-ethyl acetate (300 mL) was stirred at room temperature for 15 hrs. The reaction mixture was concentrated, diethyl ether was added to the residue to allow precipitation of crystals, and crystals were collected by filtration. A mixture of the obtained crystal, tetrahydrofuran (500 mL) and thionyl chloride (14.16 g) was heated under reflux for 2 hrs. The reaction mixture was concentrated and ethyl acetate was added to the residue. The ethyl acetate layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The obtained residue was subjected to silica gel column chromatography and eluted with ethyl acetate-hexane (1:6, v/v) to give ethyl 5-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)thiophene-2-carboxylate as colorless crystals (5.41 g, yield 24%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 101-102° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07368578B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-153c4d47d5ca4274ba664f148409f6ca
출처 메모uspto-grants-2008_05