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HRID 1638465作成日:2026年10月26日

N-(4-fluorophenyl)acetamide → 4-Fluoro-N-(4-fluorophenyl)benzenamine

https://huagongshe.com/reaction/1638465

反応式

関与物質

役割名称HCID仕込み量
反応物N-(4-fluorophenyl)acetamideHCID 9601—
反応物1-Bromo-4-fluorobenzeneHCID 9993—
反応物Potassium CarbonateHCID 11430—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物4-Fluoro-N-(4-fluorophenyl)benzenamineHCID 11241173—

反応手順

A mixture of p-fluoroacetanilide (76.5 g, 0.5 mole), 4-bromofluorobenzene (262.5 g, 1.5 mole), K2CO3 (76 g, 0.55 mole), Cu2Br2 (157.8 g, 0.55 mole) and N-methylpyrrolidone (600 ml) were heated at 175°-180°. After allowing low boiling material to condense off, the mixture was heated at reflux for 7 days. The mixture was cooled to 60° and quenched into a mixture of 2 liters H2O, 600 ml ethylenediamine and 1.2 liters toluene, filtered and the toluene layer separated, back-washed 2×600 ml H2O, treated with activated carbon, dried over MgSO4 and concentrated to oil solids in vacuo. The latter were taken up in 1.5 liters 10% ethanolic KOH, refluxed 18 hours and concentrated in vacuo to an oil. The oil was partitioned between 750 ml H2O and 750 ml. ether. The water layer was washed 2× 200 ml ether. The organic layers were combined, back-washed 2×200 ml H2O, treated with activated carbon, dried over MgSO4, reconcentrated to an oil (60.3 g) and distilled to yield purified title product 41.6 g, b.p. 158°-160°/2 mm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04879391
出典データセットuspto-grants-1989_11
ORD IDord-dd53e117f39548aeb46f9db20235e8f9
出典メモuspto-grants-1989_11