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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 875186생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/875186

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물4-Methyl-1,3-oxazole-5-carboxylic acidHCID 292311—
용매TetrahydrofuranHCID 8028—
용매Thionyl ChlorideHCID 24386—
생성물N-Methoxy-N,4-dimethyloxazole-5-carboxamideHCID 1892536948.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08981111B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-641a01cec1a04a67a708091d1e324a34
출처 메모uspto-grants-2015_03