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HRID 574046作成日:2026年10月26日

6-Aminohexanoic Acid → 6-(5-Nitro-1,3-dioxo-2,3-dihydro-1h-benzo[de]isoquinolin-2-yl)hexanoic acid

https://huagongshe.com/reaction/574046

反応式

関与物質

役割名称HCID仕込み量
反応物6-Aminohexanoic AcidHCID 564—
反応物Naphthalic anhydride, 3-nitro-HCID 18194—
生成物6-(5-Nitro-1,3-dioxo-2,3-dihydro-1h-benzo[de]isoquinolin-2-yl)hexanoic acidHCID 9906684—

反応手順

2.45 g (0.01 mmol) of 5-nitro-1H,3H-benzo[de]isochromene-1,3-dione and 1.23 g (0.01 mmol) of 6-aminohexanoic acid was alloyed with at 210-220° C. for 35 min. The obtained crude 6-(5-nitro-1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinolin-2-yl)hexanoic acid was recrystallized from ethanol. Yield 1.7 g (48%). The product was dissolved in 50 mL of ethanol and was added dropwise to the hot solution of 8 g of tin chloride in 9 mL of hydrochloric acid at boiling. The reaction mixture was boiled for 4 h, then poured with water and neutralized with 5% solution of sodium hydrate. Yellow sediment was filtered and purified by a column chromatography (Silica gel, chloroform). Yield 1.1 g of ethyl 6-(5-amino-1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinolin-2-yl)hexanoate (31.5% counting on 5-nitro-1H,3H-benzo[de]isochromene-1,3-dione). M.P. 108-110° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09034655B2
出典データセットuspto-grants-2015_05
ORD IDord-5da095d64c894c8ea2d4b4466471ef12
出典メモuspto-grants-2015_05