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HRID 270141作成日:2026年10月25日

Dimethylformamide → Ethyl 4-(hydroxymethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/270141

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物4-Bromomethyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic Acid Ethyl EsterHCID 17951768—
触媒Silver trifluoroacetateHCID 76299—
生成物Ethyl 4-(hydroxymethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carboxylateHCID 17951856—

反応手順

To a stirred solution of ethyl 4-(bromomethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carboxylate (50g, 0.127moles, 1eq) in dry DMF (300ml) under a positive N2flow was added silver trifluoroacetate (42.02g, 0.191moles, 1.5eq) all at once as a solid. This was stirred at room temperature for 3.5hrs. The reaction was partitioned between ethyl ether (1.5L) and water (500ml). The phases were separated and the organic phase washed twice with water (500ml). After separation of the phases, the organic fraction was dried with Na2SO4, filtered and concentrated in vacuo. The crude trifluoroacetate product was used without characterization. Ethanol (300ml) was added and the reaction was refluxed for 10hrs. After cooling to room temperature the ethanol was removed in vacuo to yield 42g (100%) of the title compound. The product was used without purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449468B2
出典データセットuspto-grants-2008_11
ORD IDord-84103e99eb8f405e9db2c76f2e4b7ca6
出典メモuspto-grants-2008_11