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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 564생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/564

반응식

참여 물질

역할이름HCID투입량
반응물2-BromoanisoleHCID 11358—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
시약Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(2-methoxyphenyl)piperazine-1-carboxylateHCID 1356054862.37%

반응 조건

온도100 °C

반응 단계

TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.059 g, 0.06 mmol) and 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.080 g, 0.13 mmol) were mixed in toluene (10 mL) and degessed at 90 °C for 10 mins. The mixture was then cooled and 1-bromo-2-methoxybenzene (0.400 mL, 3.21 mmol), sodium 2-methylpropan-2-olate (0.493 g, 5.13 mmol) and tert-butyl piperazine-1-carboxylate (0.597 g, 3.21 mmol) were added. The resulting mixture was stirred at 100 °C for 16 hours under nitrogen. The reaction mixture was filtered through celite and the filtrate concentrated. The crude product was purified by flash silica chromatography, elution gradient 20 to 100% EtOAc in heptane. Pure fractions were evaporated to dryness to afford tert-butyl 4-(2-methoxyphenyl)piperazine-1-carboxylate (0.585 g, 62.4 %) as a yellow oil which crystallised on standing.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-636da506499347d7aba99b6e3204f5ba
출처 메모750 AstraZeneca ELN dataset