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HRID 369591作成日:2026年10月24日

Triethylamine → 6-Fluoro-3-methyl-1,2-benzoxazole

https://huagongshe.com/ja/reaction/369591

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物4'-Fluoro-2'-hydroxyacetophenoneHCID 2737326—
溶媒TetrahydrofuranHCID 8028—
生成物6-Fluoro-3-methyl-1,2-benzoxazoleHCID 21978409—

反応手順

A mixture of 4'-fluoro-2'-hydroxyacetophenone, oxime (47.0 g, 0.278 mol) in tetrahydrofuran is heated to just under reflux, treated with a solution of 1,1'-carbonyldiimidazole (55.0 g, 0.340 mol) and triethylamine (39.0 g, 0.390 mol) in tetrahydrofuran, refluxed for one hour, cooled, concentrated in vacuo, and poured into an ice-water mixture. The resultant aqueous mixture is extracted with ether. The organic extracts are combined, washed sequentially with saturated ammonium chloride solution and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain an oil. Column chromatography of the oil using silica gel and a methylene chloride/hexanes solution (1:1) gives the title product as a yellow oil which is identified by 1H NMR spectral analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06140270
出典データセットuspto-grants-2000_10
ORD IDord-02560b88b2444856aaeaa5ab1eef6c63
出典メモuspto-grants-2000_10