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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 538528생성일: 2026년 10월 26일

Potassium Carbonate → 3-[(5-Methyl-3-pyridinyl)methoxy]benzenecarboxamide

https://huagongshe.com/reaction/538528

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3,5-DimethylpyridineHCID 11565—
반응물N-bromobutanimideHCID 67184—
반응물3-HydroxybenzamideHCID 342403—
용매Carbon TetrachlorideHCID 5943—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물3-[(5-Methyl-3-pyridinyl)methoxy]benzenecarboxamideHCID 594030127.2%

반응 단계

N-Bromosuccinimide (2.13 g, 12 mmol) and subsequently α,α′-azoisobutyronitrile (16 mg, 0.1 mmol) were added to a solution of 3,5-lutidine (1.14 ml, 10 mmol) in CCl4 (40 ml). The reaction mixture was stirred at reflux for 2 hrs. After cooling, succinimide was removed by filtration and the filtrate was evaporated to smaller volume (10 ml). To this filtrate, a mixture of 3-hydroxybenzenecarboxamide (550 mg, 4 mmol) and K2CO3 (830 mg, 6 mmol) in DMF (5 ml) was added and the new reaction mixture was stirred at 60° C. for 24 h. After diluting with CH2Cl2 (100 ml), the solution was washed with Na2CO3 solution (40 ml) and water (40 ml), dried (Na2SO4) and evaporated to dryness, under reduced pressure. The brown oil residue was extracted by trituration with Et2O (2×10 ml), and from the Et2O extracts, the precipitant solid was filtered and washed with pentane, to give 70 mg (7.2% yield) of the desired product. Mp 152-154° C., HPLC-MS: m/z 243 [M+H]+, Rt=2.28 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865736B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-893585267d384c23bc61c5c76b22ceee
출처 메모uspto-grants-2014_10