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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1258584생성일: 2026년 10월 25일

p-Toluenesulfonic acid → 6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridine-2-carbaldehyde

https://huagongshe.com/reaction/1258584

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참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물N-{[6-(1,3-dioxolan-2-yl)pyridin-2-yl]methoxy}-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimineHCID 86653136—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridine-2-carbaldehydeHCID 86653137106.9%

반응 조건

온도100 °C

반응 단계

To a solution of N-{[6-(1,3-dioxolan-2-yl)pyridin-2-yl]methoxy}-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine (3.3 g, 9 mmol, 1 eq.) in 75 ml of DMSO and 15 ml of water was added p-TSA (1.79 g, 9.45 mmol, 1.05 eq.). The reaction was heated to 100° C. for 1.5 hrs. After cooling to room temperature, the mixture was diluted with 400 ml of EtOAc, washed with sat. aqueous NaHCO3, followed by water (×2). The organic layer was separated, dried over MgSO4 and concentrated to give 6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridine-2-carbaldehyde (3.1 g, 96% yield) as a viscous yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466176B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-31e536262a7041e281c21674b3d64591
출처 메모uspto-grants-2013_06