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HRID 270663作成日:2026年10月27日

Toluene → 3-[2-(3-Chlorophenyl)ethyl]-2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)-pyridine

https://huagongshe.com/reaction/270663

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物TetrahydrofuranHCID 8028—
反応物m,alpha-DichlorotolueneHCID 12103—
反応物OxazolineHCID 68157—
反応物Lithium diisopropylamideHCID 2724682—
溶媒WaterHCID 962—
生成物3-[2-(3-Chlorophenyl)ethyl]-2-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)-pyridineHCID 1026778580.2%

反応条件

温度0 °C

反応手順

521.7 ml of anhydrous THF and 521.7 ml of 2M LDA solution (1.04 mol) are placed in a 3-litre jacketed reactor equipped with a mechanical stirrer and thermometer, and maintained under a nitrogen atmosphere, the internal temperature is brought to −5° C. and a solution consisting of 158.8 g of oxazoline (0.835 mol) and 834.7 ml of anhydrous THF is then added slowly, keeping the temperature at about 0° C. After adding a few drops of solution, a strong blue-violet colour is obtained. The total addition time is about one hour. 154.6 g (0.96 mol) of 3chlorobenzyl chloride are then added over about 1.5 hours, while still maintaining the temperature at 0° C. At the end of the reaction, 521.7 g of water are added while bringing the temperature to 20-25° C. The two phases are then separated and the organic phase is evaporated to give an oil. The crude product thus obtained is taken up in toluene and filtered through Tonsil. The filtrate is concentrated to give 268.1 g of an oil with an HPLC titre of 79%. 91.8% conversion, yield=80.2%

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449583B2
出典データセットuspto-grants-2008_11
ORD IDord-2e436d3a1b6946028cfc74c1f83c2db0
出典メモuspto-grants-2008_11