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HRID 221055作成日:2026年10月26日

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

https://huagongshe.com/reaction/221055

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物ChlorosuccinimideHCID 31398—
反応物5-Ethyl-2-thiophenecarboxaldehydeHCID 169830—
溶媒DimethylformamideHCID 6228—
生成物4-Chloro-5-ethyl-2-thiophenecarboxaldehydeHCID 8387431641.5%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202984B2
出典データセットuspto-grants-2012_06
ORD IDord-013185b1457e450d8cb505bf2cd60f3f
出典メモuspto-grants-2012_06