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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1855503생성일: 2026년 10월 26일

2-Methylthiazole → 5-(2-Methoxy-4-nitro-phenyl)-2-methyl-thiazole

https://huagongshe.com/reaction/1855503

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylthiazoleHCID 77129—
반응물2-Bromo-5-nitroanisoleHCID 101293—
반응물Potassium AcetateHCID 517044—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매DimethylacetamideHCID 31374—
생성물5-(2-Methoxy-4-nitro-phenyl)-2-methyl-thiazoleHCID 6709635242.6%

반응 단계

In a microwave vial a mixture of 2-bromo-5-nitroanisole (800 mg, 3.38 mmol), potassium acetate (503 mg, 5.07 mmol) and tetrakis(triphenylphosphine)-palladium(0) (197 mg, 0.17 mmol) in N,N-dimethylacetamide (12 mL) were flushed with argon while 2-methylthiazole (1.71 g, 16.9 mmol) was added. The tube was sealed and the mixture irradiated two times for 30 minutes at 160° C. The red-brown mixture was partitioned between ethyl acetate and water. The water layer was re-extracted with ethyl acetate. The combined organic phases were washed three times with water, once with brine, dried with magnesium sulfate and evaporated to dryness. Column chromatography (70 g silica, heptane/ethyl acetate 7:3 v/v) afforded the title compound (360 mg, 42%) as a yellow solid. MS ISP (m/e): 251.1 [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=8.15 (s, 1H), 7.90 (dd, 1H), 7.84 (s, 1H), 7.72 (d, 1H), 4.05 (s, 3H), 2.76 (s, 3H). Mp 114-117° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962834B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-59722fd22d2b444ca30c33e4a0d2bbe5
출처 메모uspto-grants-2015_02