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HRID 11181作成日:2026年10月25日

Dimethyl Sulfoxide → 2-Bromo-9,9-di-n-octylfluorene

https://huagongshe.com/reaction/11181

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物1-BromooctaneHCID 8140—
反応物2-Bromo-9H-fluoreneHCID 14336—
反応物Sodium HydroxideHCID 14798—
触媒Benzyl triethylammonium chlorideHCID 66133—
溶媒HexaneHCID 8058—
溶媒Diethylether waterHCID 21584184—
生成物2-Bromo-9,9-di-n-octylfluoreneHCID 12964693155.4%

反応手順

A 3L flask fitted with a mechanical stirrer was charged with 2-bromofluorene (45 g, 183.6 mmole) and 150 mL DMSO. Under a N2 atmosphere was added 80 mL of a 50% aqueous NaOH solution and 2.72 g of benzyltriethylammonium chloride (2.72 g, 11.98 mmole). This was stirred for 2 h at RT. With vigorous mechanical stirring, n-octylbromide (84.96 g, 440 mmole) was added via a dropping funnel (exotherm). Stirring was continued for 2 hours. To the reaction mixture was added 500 mL of a 1:1 mixture of water/ether, and the organic layer separated and was washed successively with brine and then water. Drying over magnesium sulfate and evaporation of the solvent gave an oil. Purification by column chromatography (silica gel; hexane as the mobile phase) gave 67 g (78% yield) of 2-bromo-9,9-dioctylfluorene as a pale oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094902B2
出典データセットuspto-grants-2006_08
ORD IDord-07d99d444aa441219797fc1437284320
出典メモuspto-grants-2006_08