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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234751생성일: 2026년 10월 24일

2-Chlorophenol → 2,5-Cyclohexadien-1-one, 2-chloro-4-((4-(diethylamino)-2-methylphenyl)imino)-

https://huagongshe.com/ko/reaction/234751

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참여 물질

역할이름HCID투입량
반응물2-ChlorophenolHCID 7245—
반응물Sodium CarbonateHCID 10340—
반응물N,N-Diethyltoluene-2,5-diamine hydrochlorideHCID 108623—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물2,5-Cyclohexadien-1-one, 2-chloro-4-((4-(diethylamino)-2-methylphenyl)imino)-HCID 10967590%

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온도55 °C

반응 단계

1450 parts K3Fe(CN)6, 595 parts Na2CO3, and 4150 parts water were added to a 12-liter round bottom flask equipped with a mechanical stirrer, thermometer, and addition funnel. The mixture was heated to 55° C. with stirring. A solution of 227 parts 4-(N,N-diethylamino)-2-methylaniline monohydrochloride, 128 parts o-chlorophenol, 1960 parts ethanol, and 2500 parts water was charged to the addition funnel and added dropwise to the stirred, heated solution. After the addition was complete the reaction mixture was maintained at 55° C. with stirring for 20 minutes. The warm mixture was filtered with vacuum and the resulting filter cake was placed in a solution of 296 parts ethanol and 1125 parts water to form a slurry. The dye was isolated by vacuum filtration. This process was repeated two times, first with 296 parts ethanol and 1125 parts water, then with 608 parts methanol. After the final vacuum filtration the filter cake was dried at 40° C. under vacuum for 48 hours. Yield was ~90%. The final product can be recrystallized from ethyl acetate or ethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05596025
출처 데이터셋uspto-grants-1997_01
ORD IDord-084edde874f649ec9ddd0f2e85d1e229
출처 메모uspto-grants-1997_01