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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351667생성일: 2026년 10월 26일

1,4-Dioxane → 1-Amino-4-[3-(morpholin-4-yl)phenyl]naphthalene

https://huagongshe.com/reaction/351667

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물4-Bromo-1-naphthylamineHCID 75303—
촉매HCID 178418397HCID 178418397—
생성물1-Amino-4-[3-(morpholin-4-yl)phenyl]naphthaleneHCID 1208527538%

반응 조건

온도100 °C

반응 단계

The above intermediate (1.49 g, 3.51 mmol) and 1-amino-4-bromonaphthalene (0.69 g, 3.11 mmol) were dissolved in 20 mL anhydrous 1,4-dioxane in a sealable tube under inert gas atmosphere. The solution was degased and purged with nitrogen (2×). Tetrakis(triphenylphosphine)palladium(0) (0.21 g, 0.18 mmol) was added and the solution was degassed and purged with nitrogen again (2×). The tube was sealed and heated to 100° C. for 17 h. After cooling to room temperature the mixture was diluted with EtOAc, saturated aqueous potassium carbonate solution (10 mL) was added and the mixture was stirred for 1 h at room temperature. The mixture was filtered over diatomaceous earth and the layers were separated. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), filtered and evaporated to dryness. Purification of the residue by flash chromatography afforded 0.363 g (1.19 mmol, 38%) of title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743788B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-f8a3525846e6472391e56daff4f1a631
출처 메모uspto-grants-2004_06