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HRID 875186作成日:2026年10月26日

Dimethylformamide → N-Methoxy-N,4-dimethyloxazole-5-carboxamide

https://huagongshe.com/reaction/875186

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物4-Methyl-1,3-oxazole-5-carboxylic acidHCID 292311—
溶媒TetrahydrofuranHCID 8028—
溶媒Thionyl ChlorideHCID 24386—
生成物N-Methoxy-N,4-dimethyloxazole-5-carboxamideHCID 1892536948.1%

反応手順

To a stirred solution of 4-methyl-1,3-oxazole-5-carboxylic acid (4.00 g, 31.5 mmol) in thionyl chloride (4 ml) were added 0.4 ml N,N-dimethylformamide and the mixture was refluxed for 2 hours. After cooling, the volatiles were removed in vacuo and the remaining material was suspended in tetrahydrofuran (10 ml). This suspension was added to a stirred suspension of N,O-dimethyl-hydroxylamine hydrochloride (3.38 g, 34.6 mmol) and triethylamine (9.55 g, 94.4 mmol) in tetrahydrofuran (10 ml). The reaction mixture was stirred at room temperature for 20 h. After evaporation of the solvent in vacuo dichloromethane and 1N HCl were added. The phases were separated, the organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. Purification of the crude material on silica gel afforded N-methoxy-N,4-dimethyl-1,3-oxazole-5-carboxamide (2.58 g, 45%) as an orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08981111B2
出典データセットuspto-grants-2015_03
ORD IDord-641a01cec1a04a67a708091d1e324a34
出典メモuspto-grants-2015_03