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HRID 1246271作成日:2026年10月26日

Potassium Carbonate → 2-Propyl-3-propyl-5-fluoro-1H-indole

https://huagongshe.com/reaction/1246271

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-OctyneHCID 16029—
反応物2-Bromo-4-fluoroanilineHCID 242873—
触媒palladium(II) acetateHCID 167845—
触媒1,1'-Bis(di-tert-butylphosphino)ferroceneHCID 71310544—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-Propyl-3-propyl-5-fluoro-1H-indoleHCID 2191662480.9%

反応条件

温度130 °C

反応手順

A 50 mL three neck flask was charged with palladium acetate (22.4 mg, 0.1 mmol), dtbpf (94 mg, 0.2 mmol), potassium carbonate (690 mg, 5 mmol), 2-bromo-4-fluoroaniline (380 mg, 2 mmol), 4-octyne (264 mg, 2.4 mmol) and NMP (10 ml). The mixture was purged with argon and heated to 130° C. After 1 hr, the reaction mixture was cooled to rt. Ethyl acetate and water were added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic phases were washed with water, brine and dried with MgSO4. Removal of the solvents and purification of the crude by column chromatography afforded the desired product as yellow oil (355 mg, containing 4.3 wt % AcOEt). The corrected yield was 77.6%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07126009B2
出典データセットuspto-grants-2006_10
ORD IDord-ee56f80cf6cf40bfa928dffb2d2f4444
出典メモuspto-grants-2006_10