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HRID 461878作成日:2026年10月26日

1,2-Dibromobenzene → 1-(4-Bromophenoxy)-3,5-di-tert-butylbenzene

https://huagongshe.com/reaction/461878

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DibromobenzeneHCID 11414—
反応物Sodium hydrideHCID 24758—
反応物3,5-Di-tert-butylphenolHCID 70825—
触媒CopperHCID 23978—
溶媒DimethylacetamideHCID 31374—
生成物1-(4-Bromophenoxy)-3,5-di-tert-butylbenzeneHCID 20321363—

反応手順

To a suspension of 8.8 g. of 50% sodium hydride (mineral oil dispersion) in 320 ml. of dry dimethylacetamide is added, in portions over 15 minutes with vigorous stirring, 32 g. of 3,5-di-tertiary butylphenol, during which the reaction mixture is cooled with an icebath to moderate the internal temperature. The reaction mixture is then stirred at room temperature for 1 hour, after which is added 75.2 g. of dibromobenzene and 800 mg. of copper powder. The resultant mixture is refluxed for 8 hours, after which time it is cooled and the dimethylacetamide is removed in vacuo. The resultant residue is extracted several times with methylene chloride and the insoluble copper filtered off. The combined methylene chloride extracts are washed two times with water, dried over sodium sulfate, filtered, evaporated in vacuo to dryness and the residue recrystallized from ethanol to obtain 1-(3,5-di-tertiary butylphenoxy)-4-bromobenzene, m.p. 98°-100° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04064273
出典データセットuspto-grants-1977_12
ORD IDord-bdff0af48ec0419193c4bbbeea246f7d
出典メモuspto-grants-1977_12