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HRID 655作成日:2026年10月23日

2-Chloroanisole → Tert-butyl 4-(2-methoxyphenyl)piperazine-1-carboxylate

https://huagongshe.com/ja/reaction/655

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChloroanisoleHCID 13011—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
試薬Sodium t-butoxideHCID 23676156—
触媒Palladium (II) acetateHCID 4144353—
触媒2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
溶媒TolueneHCID 1140—
生成物Tert-butyl 4-(2-methoxyphenyl)piperazine-1-carboxylateHCID 1356054811.22%

反応条件

温度100 °C

反応手順

RuPhos (32.7 mg, 0.07 mmol) and palladium (II) acetate (15.75 mg, 0.07 mmol) were suspended in toluene (1 mL) at ambient temperature. The mixture was degassed and purged with nitrogen several times and warmed to 50°C for 20 mins. In a separate vessel were mixed 1-chloro-2-methoxybenzene (100 mg, 0.70 mmol), tert-butyl piperazine-1-carboxylate (131 mg, 0.70 mmol), sodium tertbutoxide (101 mg, 1.05 mmol) and toluene (2 mL). The suspension was degassed and purged with nitrogen then warmed to 50°C. The solution of catalyst was added to the reaction vessel and the resulting mixture was degassed and purged with nitrogen. The reaction was heated to 110°C (ext T) under nitrogen for 6 hours then allowed to cool to ambient temperature overnight. The reaction mixture was filtered and concentrated and the crude material purified by flash silica chromatography, elution gradient 20 to 60% EtOAc in heptane. Pure fractions were evaporated to dryness to afford tert-butyl 4-(2-methoxyphenyl)piperazine-1-carboxylate (23.00 mg, 11.22 %) as a colourless dry film. Yield not good....if this route followed maybe try different catalyst - pepsi?

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-7d6438f5772442a8addd4f9357140a8b
出典メモ750 AstraZeneca ELN dataset