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HRID 921601作成日:2026年10月26日

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

https://huagongshe.com/reaction/921601

反応式

関与物質

役割名称HCID仕込み量
反応物CarbazoleHCID 6854—
反応物Benzene, 1-bromo-3-iodo-HCID 11561—
反応物Sodium t-butoxideHCID 23676156—
触媒Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
生成物9-(3-bromophenyl)-3,6-diphenyl-9H-CarbazoleHCID 58142231—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09276217B2
出典データセットuspto-grants-2016_03
ORD IDord-c1a5272316a74904a40229974293cdfc
出典メモuspto-grants-2016_03