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HRID 217561作成日:2026年10月26日

Dioctylamine → 4,4'-Bis-dioctylaminostilbene

https://huagongshe.com/reaction/217561

反応式

関与物質

役割名称HCID仕込み量
反応物DioctylamineHCID 3094—
反応物(2-Methylphenyl)phosphaneHCID 15049146—
反応物Sodium t-butoxideHCID 23676156—
反応物4,4'-DibromostilbeneHCID 53395981—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物4,4'-Bis-dioctylaminostilbeneHCID 54430651—

反応条件

温度80 °C

反応手順

An oven dried 3-necked flask was fitted with a reflux condenser and purged with nitrogen. Into the flask was placed 4,4′-dibromostilbene (1.0 g, 2.96 mmol) (synthesized by the general Wittig procedure described above), tris(dibenzylideneacetone)dipalladium (Pd2(dba)3) (13.5 mg, 0.0148 mmol), o-tolylphosphine (13,5 mg, 0.044 mmol), and sodium t-butoxide (711 mg, 7.4 mmol) in 6 mL dry toluene. Dioctylamine (1.608 g, 6.65 mmol) was then added and the reaction mixture was stirred for 48 hours at 80° C. under nitrogen balloon atmosphere. The crude product was then adsorbed onto silica gel and purified via flash chromatography with gradual elutions from 98/2 to 95/5 (hexanes:ethyl acetate). 1H NMR (d6-acetone) δ 0.89 (m, 12H), 1.20-1.70 (m, 24H), 3.34 (t, J=7.51 Hz, 8H), 6.66 (d, J=8.75 Hz, 4H), 6.83 (s, 2H), 7.32 (d, J=8.62 Hz, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08197722B2
出典データセットuspto-grants-2012_06
ORD IDord-62d3fd38ea904077ab269bbf844adb6f
出典メモuspto-grants-2012_06