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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 921601생성일: 2026년 10월 25일

Carbazole → 9-(3-bromophenyl)-3,6-diphenyl-9H-Carbazole

https://huagongshe.com/reaction/921601

반응식

참여 물질

역할이름HCID투입량
반응물CarbazoleHCID 6854—
반응물Benzene, 1-bromo-3-iodo-HCID 11561—
반응물Sodium t-butoxideHCID 23676156—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물9-(3-bromophenyl)-3,6-diphenyl-9H-CarbazoleHCID 58142231—

반응 단계

Mix together 0.4 g Pd2DBA3 and 0.4 g DPPF and 4.3 g sodium t-butoxide and dissolve into 200 mL xylenes in glove box. Stir 15 mins then add 25 g of 3-iodo-bromobenzene. Stir 15 mins then add 10 g carbazole and the mix brought to reflux. Reflux o/n. using an air condensor. Solution immediately is dark purple/brown but on reaching ˜80 C. it is dark reddish brown and cloudy. After heating close to reflux overnight, the solution is dark brown and clear. Evaporated outside the glove box in rotovap and then dissolved in DCM and extracted (soxhlet) through a bed of silica and basic alumina (stacked in soxhlet) using DCM. Collect dark orange solution and evaporate to dryness. Leaves a dark orange oil. Wash with methanol and then dissolve into ether and reprecipitate with methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09276217B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-c1a5272316a74904a40229974293cdfc
출처 메모uspto-grants-2016_03