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HRID 532631생성일: 2026년 10월 25일

Sodium hydride → 2-Bromo-6-(4-methoxy-phenyl)-4-(2-trimethylsilanyl-ethoxymethyl)-4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalene

https://huagongshe.com/reaction/532631

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
반응물2-Bromo-6-(4-methoxy-phenyl)-4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentaleneHCID 71816014—
용매TetrahydrofuranHCID 8028—
생성물2-Bromo-6-(4-methoxy-phenyl)-4-(2-trimethylsilanyl-ethoxymethyl)-4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentaleneHCID 8669923079.2%

반응 조건

온도0 °C

반응 단계

At 0° C., NaH (60 percent, 1.3 g, 33 mmol) was added to a THF solution (40 mL) containing 2-Bromo-6-(4-methoxy-phenyl)-4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalene (8.3 g, 24 mmol). Then SEM-Cl (5.6 mL, 28 mmol) was added to the reaction mixture and the resulting mixture was stirred at 0° C. for 30 min, warmed up to 80° C. and stirred for 2 hr. The solution was cooled to room temperature and poured into ice water. The resulting mixture was extracted with ethyl acetate. The organic layer was collected and washed with saturated aqueous NH4Cl, dried over MgSO4(s), and concentrated under reduced pressure. The oily residue was purified by gravity column chromatography (20% ETOAc in hexane) to give 2-Bromo-6-(4-methoxy-phenyl)-4-(2-trimethylsilanyl-ethoxymethyl)-4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalene (9.0 g, 19.0 mmol) as brown solid in 79% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853207B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-2b0c147ce6c0454584ec7e3f22f94070
출처 메모uspto-grants-2014_10