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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1441849생성일: 2026년 10월 24일

Triethylamine → 3-Methoxypyridine-2-carbonitrile

https://huagongshe.com/ko/reaction/1441849

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Pyridine, 3-methoxy-, 1-oxideHCID 139850—
용매AcetonitrileHCID 6342—
생성물3-Methoxypyridine-2-carbonitrileHCID 11332493—

반응 단계

3-Methoxypyridine-1-oxide (25.2 g, 209 mmol) was dissolved in acetonitrile (260 mL). Trimethylsilycyanide (66.35 g, 669 mmol) and triethylamine (45.13 g, 446 mmol) were added and the reaction mixture heated at reflux for overnight. The cooled solution was concentrated in vacuo to give a brown solid which was partitioned between CH2Cl2 and 3M Na2CO3. The organic layer was separated, washed with brine, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by silica gel chomatography using 1:1 EtOAc/hexanes as eluent. Compound 762B was isolated (17.63 g, 63%) as a light yellow solid. HPLC: 96.2% at 1.37 min(YMC S5 ODS column) eluting with 10-90% aqueous methanol containing 0.2% phosphoric acid over a 4 min gradient monitoring at 220 nm. MS (ES): m/z 134.88 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07655689B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-2b37939d31d241f7a4f029c025060f55
출처 메모uspto-grants-2010_02