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HRID 1644721作成日:2026年10月25日

Ethyl Acetate → [6-Fluoro-4-(4-methanesulfonyl-benzoyl)-naphthalen-2-yl]-acetic acid ethyl ester

https://huagongshe.com/reaction/1644721

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物1,4-DioxaneHCID 31275—
反応物Ethyl 4-oxobutanoateHCID 82395—
反応物4-Fluoro-2-(4-methanesulfonyl-phenylethynyl)-benzaldehydeHCID 59350830—
触媒Gold tribromideHCID 82525—
溶媒HexaneHCID 8058—
生成物[6-Fluoro-4-(4-methanesulfonyl-benzoyl)-naphthalen-2-yl]-acetic acid ethyl esterHCID 5935081126%

反応条件

温度100 °C

反応手順

To a mixture of 4-fluoro-2-(4-methanesulfonyl-phenylethynyl)-benzaldehyde (1.74 g, 5.77 mmol) and gold(III) bromide (0.15 g, 0.35 mmol) in dioxane (8 mL) was added 4-oxo-butyric acid ethyl ester (1.50 g, 11.53 mmol). The reaction mixture was heated at 100° C. under nitrogen for 4 hours. The solvent was removed in vacuo to afford a deep red viscous oil. Flash chromatography (RediSep® Flash column, 230-400 mesh, 25-65% ethyl acetate in hexane) gave [6-fluoro-4-(4-methanesulfonyl-benzoyl)-naphthalen-2-yl]-acetic acid ethyl ester (0.63 g, 26%). MS (ESI+) cald. for C22H19FO5S [(M+H)+] 414, obsd. 415. It is noted that in some instances, this reaction also produced some amount of [6-fluoro-4-(4-methanesulfonyl-benzoyl)-naphthalen-2-yl]-acetic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124629B2
出典データセットuspto-grants-2012_02
ORD IDord-68f953d2e0b54005ba68116fba2e903d
出典メモuspto-grants-2012_02