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HRID 856072作成日:2026年10月25日

p-Bromochlorobenzene → Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/856072

反応式

関与物質

役割名称HCID仕込み量
反応物p-BromochlorobenzeneHCID 7806—
反応物Ethyl AcetateHCID 8857—
反応物4-Amino-1-Boc-piperidineHCID 1268291—
反応物Sodium t-butoxideHCID 23676156—
触媒palladium(II) acetateHCID 167845—
触媒Binap, (A+-)-HCID 634876—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylateHCID 149150386%

反応手順

A mixture of p-bromochlorobenzene (1.91 g, 9.99 mmol), tert-butyl 4-aminopiperidine-1-carboxylate (2.0 g, 9.99 mmol), palladium acetate (45 mg, 0.2 mmol), (R)-(+)-BINAP (187 mg, 0.3 mmol) and sodium tert-butoxide (1.35 g, 14.0 mmol) in toluene (20 ml) was refluxed under a nitrogen atmosphere for 1 hour. Ethyl acetate and water were added to the reaction mixture while stirring, the insoluble substances were removed by filtration through Celite, and the filtrate was then extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride/methanol=100/1) to afford tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate (2.67 g, yield 86%) as a yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07262212B2
出典データセットuspto-grants-2007_08
ORD IDord-c276d8dff44d4683981ae2411bdadb15
出典メモuspto-grants-2007_08