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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 406041생성일: 2026년 10월 25일

Hydrochloric Acid → 2-(cis-3-Methoxy-cyclohexyloxy)-3-nitro-pyridine

https://huagongshe.com/reaction/406041

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물2-Fluoro-3-nitropyridineHCID 2762817—
반응물HCID 178496631HCID 178496631—
생성물2-(cis-3-Methoxy-cyclohexyloxy)-3-nitro-pyridineHCID 67382506—

반응 단계

LiHMDS (1 M solution in THF; 40.0 ml) was added slowly to an ice/ethanol-cooled solution of cis/trans-4-methoxy-cyclohexanol (5.00 g) in THF (10 ml). Cooling was suspended after the addition was complete and the mixture was stirred for 15 minutes at room temperature. A solution of 2-fluoro-3-nitro-pyridine (5.10 g) in THF (10 ml) was added slowly while the temperature was maintained below 24° C. The reaction mixture was stirred for 2 h at room temperature, neutralized by addition of hydrochloric acid (1M), and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. The residue was submitted to column chromatography (silica gel, petrol ether/ethyl acetate 70:30 50:50) to give the cis-isomer (5.82 g) and the trans-isomer (1.60 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754079B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-c94aadac8c314992ae9f019e086540ae
출처 메모uspto-grants-2014_06