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HRID 544642作成日:2026年10月27日

Pyridine → 2-Ethylthio-4,5-bis-phenylthiazole

https://huagongshe.com/reaction/544642

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2-Bromo-1,2-diphenylethan-1-oneHCID 102630—
反応物EthyldithiocarbamateHCID 18544323—
溶媒EthanolHCID 702—
生成物2-Ethylthio-4,5-bis-phenylthiazoleHCID 13209657—

反応手順

1.106 g of pyridine and 3.68 g of 2-bromo-1,2-bis-phenylethanone are added while stirring to a solution, cooled to 5°, of 1.694 g of ethyldithiocarbamate in 25 ml of ethanol. The mixture is then stirred for 30 minutes at 5° and for 90 minutes at room temperature, concentrated to dryness by evaporation under reduced pressure, and the residue is partitioned between methylene chloride and water. The aqueous phase is acidified with N hydrochloric acid and extracted by shaking again twice with methylene chloride. The organic phases are combined, dried over magnesium sulphate and concentrated to dryness by evaporation under reduced pressure. The remaining oil is purified by chromatography over 100 g of silica gel with toluene/hexane (1:1) as eluant. Concentration by evaporation yields 2-ethylthio-4,5-bis-phenylthiazole in the form of an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04451471
出典データセットuspto-grants-1984_05
ORD IDord-71fb122494914043824b8ddf4b515978
出典メモuspto-grants-1984_05