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HRID 399270作成日:2026年10月25日

Trifluoroacetic anhydride → 2-((5-Methoxy-1H-indol-6-yl)oxy)-N,N-dimethylethan-1-amine

https://huagongshe.com/reaction/399270

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic anhydrideHCID 9845—
反応物N-[3-(2-dimethylaminoethoxy)4-methoxyphenyl]aminoacetaldehyde dimethyl acetalHCID 10590199—
溶媒Trifluoroacetic acidHCID 6422—
生成物2-((5-Methoxy-1H-indol-6-yl)oxy)-N,N-dimethylethan-1-amineHCID 1053765983%

反応手順

A stirred solution of N-[3-(2-dimethylaminoethoxy)4-methoxyphenyl]aminoacetaldehyde dimethyl acetal (D12, 5.3 g, 0.018 mole) in trifluoroacetic acid (22 ml) at -5° C. under argon was treated dropwise over 40 minutes with trifluoroacetic anhydride (22 ml). After a further 30 minutes the dark solution was treated with more trifluoroacetic acid (33 ml) and then heated under reflux for 7 hours. The solution was concentrated in vacuo and the residue basified with 10% Na2CO3 solution and extracted with ethyl acetate. The extract was dried (Na2SO4), concentrated in vacuo and the residue dissolved in methanol (100 ml), treated with potassium carbonate (10 g) and stirred at room temperature for 3 hours. The mixture was concentrated in vacuo,.the residue treated with water (60 ml) and extracted with ethyl acetate (2×70 ml). The combined extract was dried (Na2SO4) and concentrated in vacuo to afford the title compound as a brown solid (3.5 g, 83%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05817833
出典データセットuspto-grants-1998_10
ORD IDord-670d8d56d37444a1aff144c1f82bef7c
出典メモuspto-grants-1998_10