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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221055생성일: 2026년 10월 26일

Water → 4-Chloro-5-ethyl-2-thiophenecarboxaldehyde

https://huagongshe.com/reaction/221055

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ChlorosuccinimideHCID 31398—
반응물5-Ethyl-2-thiophenecarboxaldehydeHCID 169830—
용매DimethylformamideHCID 6228—
생성물4-Chloro-5-ethyl-2-thiophenecarboxaldehydeHCID 8387431641.5%

반응 단계

To a solution of 5-ethyl-2-thiophenecarboxaldehyde (6.0 g) in N,N-dimethylformamide (60 ml) was added N-chlorosuccinimide (8.57 g), and the mixture was stirred at room temperature for 2 hours, and subsequently stirred under heating at 60° C. for 2 hours. N-chlorosuccinimide (4.00 g) was further added thereto, and the mixture was further stirred under heating at 60° C. for 2 hours. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate, washed with brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=33:1) to give 4-chloro-5-ethyl-2-thiophenecarboxaldehyde (3.1 g) as colorless oil. (2) The above 4-chloro-5-ethyl-2-thiophenecarboxaldehyde was treated in a manner similar to Reference Example 1 to give 3-bromo-1-(4-chloro-5-ethyl-2-thienylmethyl)benzene as yellow oil. APCI-Mass m/Z 347/349 (M+H+MeOH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202984B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-013185b1457e450d8cb505bf2cd60f3f
출처 메모uspto-grants-2012_06