돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 989340생성일: 2026년 10월 25일

Acetic Acid → 7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile

https://huagongshe.com/reaction/989340

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AcetonitrileHCID 6342—
반응물ButyllithiumHCID 178418339—
반응물HCID 178496951HCID 178496951—
용매TetrahydrofuranHCID 8028—
생성물7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrileHCID 9813663—

반응 조건

온도-78 °C

반응 단계

To a solution of 4.75 mL (11.88 mmol) of n-butyllithium (2.5M in hexane) in 4.0 mL of tetrahydrofuran at −78° C. is added dropwise a solution of 0.68 mL (13.1 mmol) of acetonitrile in 6.8 mL of tetrahydrofuran. After completion of addition, the suspension is stirred for 10 minutes. To this is added 1.36 g (4.75 mmol) of methyl 3-{[(E)-(dimethylamino)methylidene]amino}-7-methoxy-2-naphthoate in 32 mL of tetrahydrofuran dropwise. The resulting reaction mixture is stirred at −78° C. for 1 hour, at −5° C. for 1 hour and at room temperature for 15 minutes. The reaction mixture is again cooled to −78° C. and 1.72 g (28.6 mmol) of acetic acid is added dropwise. After addition of the acetic acid, the reaction mixture is allowed to warm to room temperature. The precipitate is collected by filtration and washed sequentially with water, acetonitrile and methanol. After drying in vacuo, this yields 796.9 mg (67%) of 7-methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile as a deep yellow solid, mp>260° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06638929B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-e64447100648458bb0aacd9594b0b3c2
출처 메모uspto-grants-2003_10