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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536생성일: 2026년 10월 24일

4-Bromoanisole → 4-methoxy-N-(oxan-4-ylmethyl)aniline

https://huagongshe.com/ko/reaction/536

반응식

참여 물질

역할이름HCID투입량
반응물4-BromoanisoleHCID 7730—
반응물4-AminomethyltetrahydropyranHCID 2773210—
시약Sodium t-butoxideHCID 23676156—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Palladium (II) acetateHCID 4144353—
용매TolueneHCID 1140—
생성물4-methoxy-N-(oxan-4-ylmethyl)anilineHCID 6238585322.82%

반응 조건

온도80 °C

반응 단계

Palladium (II) acetate (0.090 g, 0.40 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (0.464 g, 0.80 mmol) were suspended in toluene (3 mL). The mixture was evacuated and purged with nitrogen, and warmed to 50°C. In a separate vessel, 1-bromo-4-methoxybenzene (1 g, 5.35 mmol), (tetrahydro-2H-pyran-4-yl)methanamine (0.654 mL, 5.35 mmol) and sodium-t- butoxide (0.771 g, 8.02 mmol) were suspended in toluene (7 mL). The resulting mixture was evacuated, purged with nitrogen and warmed to 50°C. After ~30 mins, the catalyst mixture was transferred to the reaction vessel. The reaction was evacuated and purged with nitrogen and heated at 80°C overnight. The mixture was diluted with water (250 mL), and extracted with ethyl acetate (200 mL). The organic was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and crude fractions were evaporated to dryness to afford 4-methoxy-N-((tetrahydro-2H-pyran-4-yl)methyl)aniline (0.270 g, 22.82 %) as a brown oil.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-c4dfba23f3204e1a90cbbf5ad1b6ca0b
출처 메모750 AstraZeneca ELN dataset