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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 600368생성일: 2026년 10월 24일

Cesium carbonate → 2-bromo-6-(6-tert-butyl-1-oxophthalazin-2(1H)-yl)benzaldehyde

https://huagongshe.com/ko/reaction/600368

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4,7-Dimethoxy-1,10-phenanthrolineHCID 10462298—
반응물2,6-DibromobenzaldehydeHCID 12648641—
반응물6-(tert-butyl)phthalazin-1(2H)-oneHCID 57633933—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매1,4-DioxaneHCID 31275—
생성물2-bromo-6-(6-tert-butyl-1-oxophthalazin-2(1H)-yl)benzaldehydeHCID 5801618569.1%

반응 단계

5.90 g (22.4 mmol) of 2,6-dibromobenzaldehyde, 1.80 g (8.90 mmol) of 6-tert-butyl-2H-phthalazin-1-one, 6.02 g (18.5 mmol) of cesium carbonate, 179 mg (0.940 mmol) of copper(I) iodide, and 428 mg (1.87 mmol) of 4,7-dimethoxy-1,10-phenanthroline were weighed into a 100 mL reaction flask fitted with a stir bar and septum cap. Added 50 mL of anhydrous dioxane. Purged the reaction mixture with nitrogen for 15 min. Stirred at 100° for 18 h. Partitioned the reaction mixture between 200 mL of 10% MeOH/CH2Cl2 and 200 mL of water. Separated phases and extracted the aqueous phase with 2×100 mL of 10% MeOH/CH2Cl2. The combined organic extracts were washed with 200 mL of brine, dried over Na2SO4, and the solvent was removed on rotavap. Purified the crude by flash chromatography on silica gel to obtain 2.37 g of the title compound as an off-white solid. MS (ESI) doublet 385, 387 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902194B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-c70dc792210a4db287e88265926eccf9
출처 메모uspto-grants-2011_03