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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 931714생성일: 2026년 10월 27일

Isopropanol → 6-Methoxy-7-methylquinoline

https://huagongshe.com/reaction/931714

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참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물3-Amino-1-propanolHCID 9086—
반응물TriphenylphosphineHCID 11776—
반응물Stannous chloride dihydrateHCID 61436—
반응물1-Methoxy-2-methyl-4-nitrobenzeneHCID 643520—
촉매Ruthenium trichloride hydrateHCID 6093376—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물6-Methoxy-7-methylquinolineHCID 1553489815.4%

반응 조건

온도180 °C

반응 단계

1-methoxy-2-methyl-4-nitrobenzene (3A) (5 g, 30.0 mmol), 3-amino-1-propanol (0.57 mL, 7.5 mmol), isopropanol (3.43 mL, 4.5 mmol), ruthenium(III) chloride hydrate (156 mg, 0.75 mmol), triphenylphosphine (588 mg, 2.24 mmol), and tin(II) chloride dihydrate (1.69 g, 7.5 mmol) in dioxane/H2O (67 mL/7 mL) were placed in a stainless steel pressure vessel. After the system was flushed with argon, the mixture was stirred at 180° C. for 20 hours. The reaction mixture was filtered through a short silica gel column (ethyl acetate/chloroform mixture) to eliminate inorganic compounds and concentrated under reduced pressure. The organic layer was poured into saturated brine, extracted with chloroform, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The residual oily material was separated by column chromatography to give the product 3B (200 mg, 15%). LCMS-ESI+ (m/z): 174.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09296758B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-777bcf34fd8e427ea76d87be20965b8e
출처 메모uspto-grants-2016_03