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HRID 561843作成日:2026年10月27日

Tributylphosphine → 2-[2-(4-Bromophenyl)ethoxy]-1,3-dichloro-5-methylbenzene

https://huagongshe.com/reaction/561843

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物2,6-Dichloro-4-methylphenolHCID 17077—
反応物2-(4-Bromophenyl)ethanolHCID 72851—
反応物1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物2-[2-(4-Bromophenyl)ethoxy]-1,3-dichloro-5-methylbenzeneHCID 66761264—

反応条件

温度80 °C

反応手順

2-(4-Bromophenyl)ethanol (1 eq.) and 2,6-dichloro-4-methylphenol (1.5 eq.) were taken up in freshly deoxygenated toluene (0.1 M). To this solution was then added 1,1′-(azodicarbonyl)-dipiperidine (1.2 eq.) and finally tributylphosphine (1.2 eq.). The resulting yellow solution was heated at 80° C. for 2 h. The reaction mixture was cooled to RT, diluted with ether, and washed with 1 N aq. NaOH. The aqueous wash was back extracted with ether and the combined organic extracts were dried over MgSO4. Filtration and concentration of the filtrate in vacuo afforded a yellow semi-solid. Purification of the crude product thus obtained by way of flash chromatography (SiO2, Hex→10:1 (v/v) Hex:EtOAc) afforded the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063105B2
出典データセットuspto-grants-2011_11
ORD IDord-8f57794e0e284dbb9b873e52c33bd924
出典メモuspto-grants-2011_11