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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 649610생성일: 2026년 10월 25일

Hydrochloric Acid → 3H-Naphtho[1,2,3-de]quinoline-1-carbonitrile, 2,7-dihydro-6-[[4-(2-hydroxyethyl)phenyl]amino]-3-methyl-2,7-dioxo-

https://huagongshe.com/reaction/649610

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Amino-alpha-methylbenzenemethanolHCID 85753—
반응물Potassium AcetateHCID 517044—
반응물3H-Naphtho[1,2,3-de]quinoline-1-carbonitrile, 6-bromo-2,7-dihydro-3-methyl-2,7-dioxo-HCID 11122075—
용매AcetoneHCID 180—
용매1-ButanolHCID 263—
생성물3H-Naphtho[1,2,3-de]quinoline-1-carbonitrile, 2,7-dihydro-6-[[4-(2-hydroxyethyl)phenyl]amino]-3-methyl-2,7-dioxo-HCID 163996—

반응 단계

A mixture of 6-bromo-1-cyano-3-methyl-3H-dibenz[f,ij]isoquinoline-2,7-dione (2.0 g), p-aminophenylethanol (15 g), potassium acetate (2.0 g), a trace of cupric acetate, and butanol (10 ml) was heated gradually to about 80° C., held for 5-10 minutes, and then drained into 250 ml of 10% HCl. The solid product was collected by filtration, washed with water, dried in air, and recrystallized twice from nitrobenzene to remove a red impurity and traces of starting material. A yield of 0.65 g of product, which had a visible absorption maximum at 587 nm in acetone, was obtained, thus imparting a reddish-blue color to acetone. The structure is as follows: ##STR6##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04740581
출처 데이터셋uspto-grants-1988_04
ORD IDord-d00e77a6b43a4d8a92c85b1e35d241b5
출처 메모uspto-grants-1988_04