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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655생성일: 2026년 10월 24일

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

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

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참여 물질

역할이름HCID투입량
반응물2-ChloroanisoleHCID 13011—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
시약Sodium t-butoxideHCID 23676156—
촉매Palladium (II) acetateHCID 4144353—
촉매2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(2-methoxyphenyl)piperazine-1-carboxylateHCID 1356054811.22%

반응 조건

온도100 °C

반응 단계

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?

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-7d6438f5772442a8addd4f9357140a8b
출처 메모750 AstraZeneca ELN dataset