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HRID 576080作成日:2026年10月27日

Sodium Hydroxide → 4-(2-Cyclopentylethyl)-2-fluoroaniline

https://huagongshe.com/reaction/576080

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物VinylcyclopentaneHCID 77345—
反応物9-Borabicyclo(3.3.1)nonaneHCID 78966—
反応物4-Bromo-2-fluoroanilineHCID 123050—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物4-(2-Cyclopentylethyl)-2-fluoroanilineHCID 8670728396.8%

反応手順

9-Borabicyclo[3,3,1]nonane (9-BBN) (tetrahydrofuran solution, 0.5 mol/L, 33 mL, 16.5 mmol) was added dropwise to a solution of vinylcyclopentane (1.59 g, 16.5 mmol) in tetrahydrofuran (7.5 mL) at 0° C. under a nitrogen atomosphere. The mixture was warmed gradually to room temperature and stirred for 15 hr. To the reaction mixture were added dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) (367 mg, 0.45 mmol), 4-bromo-2-fluoroaniline (2.85 g, 15.0 mmol) and 3 mol/L aqueous sodium hydroxide solution (15 mL, 45.0 mmol), and the mixture was heated to reflux for 10 hr. After cooling, ethyl acetate was added thereto, the mixture was filtered through Celite (registered trademark), and the filtrate was concentrated under reduced pressure. Water was added thereto, the mixture was extracted with ethyl acetate, and the organic layer was washed with brine. After drying over anhydrous magnesium sulfate, the desiccant was filtered off, followed by concentration under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to afford the title compound as a pale yellow oil (3.01 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09035059B2
出典データセットuspto-grants-2015_05
ORD IDord-27f6b73871bd4f1e91128c9653f0fb28
出典メモuspto-grants-2015_05