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HRID 47178作成日:2026年10月24日

1,2-Dibromoethane → 3,3'',5,5''-Tetra-naphthyl-p-quaterphenyl

https://huagongshe.com/ja/reaction/47178

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DibromoethaneHCID 7839—
反応物4,4'-Diiodo-1,1'-biphenylHCID 76348—
反応物MagnesiumHCID 5462224—
反応物1,1'-(5-Bromo-1,3-phenylene)dinaphthaleneHCID 22743684—
触媒HCID 178418476HCID 178418476—
溶媒TetrahydrofuranHCID 8028—
生成物3,3'',5,5''-Tetra-naphthyl-p-quaterphenylHCID 2274368681%

反応条件

温度60 °C

反応手順

A solution of 3,5-di-α-naphthyl bromobenzene (10.0 g, 0.0244 mol) in anhydrous THF (70 mL) was added dropwise to magnesium turnings (0.59 g, 0.0244 mol) in 10 mL THF. The solution was heated at 60° C. during the addition and the reaction was initiated using 1,2-dibromoethane. After the addition was complete, the brown solution was heated at reflux for 2 hrs. and then cooled to room temperature. In a separate flask, 4,4′-diiodobiphenyl (3.3 g 0.008 mol) and 0.3 g of dichlorobis(triphenyl phosphine)palladium(II) were placed under nitrogen and 30 mL of anhydrous THF was added. The Grignard reagent prepared about THF solution was then added using needle-transfer and an orange solution resulted. Heat was applied and the solution turned to almost black. The mixture was then heated at reflux for 45 min. and cooled to room temperature during which time a solid precipitated out of solution. A 2.0 M solution of HCl was added to the mixture and after stirring for 30 minutes, the water layer was removed. The solid precipitate was collected by filtration and washed with water and diethyl ether to yield a white solid (5.3 g, 81%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699595B2
出典データセットuspto-grants-2004_03
ORD IDord-12c65c39c56a4a428c86722dd8dd49d5
出典メモuspto-grants-2004_03