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HRID 910769作成日:2026年10月27日

Water → Ethyl 1-[3-bromoprop-2-en-1-yl]-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate

https://huagongshe.com/reaction/910769

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物1,3-DibromopropeneHCID 5201028—
反応物Ethyl 4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylateHCID 12876362—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 1-[3-bromoprop-2-en-1-yl]-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylateHCID 72343106—

反応手順

Ethyl-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate (714 mg, 3.04 mmol) was suspended in degassed N,N-dimethylformamide (8 mL) and treated with 1,3-dibromo-1-propene (0.364 mL, 3.64 mmol, 1.2 equiv) and potassium carbonate (503 mg, 3.64 mmol, 1.2 equiv). After stirring for 7 hrs at ambient temperature, the mixture was poured into water and extracted three times with ethyl acetate. The combined ethyl acetate extracts were washed once with water and brine, dried with sodium sulfate, filtered and concentrated in vacuo to afforded ethyl 1-[3-bromoprop-2-en-1-yl]-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate as a mixture of E- and Z-isomers. Additional compound was obtained by concentration of the aqueous extract in vacuo and extraction of the resulting residue with a mixture of 80% chloroform and 20% methanol (v/v).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08022215B2
出典データセットuspto-grants-2011_09
ORD IDord-55a7999a8f44485ba64ad45c3368732a
出典メモuspto-grants-2011_09