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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 399178생성일: 2026년 10월 23일

Sodium Hydroxide → Quinacridone

https://huagongshe.com/ko/reaction/399178

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Sodium 3-nitrobenzenesulfonateHCID 31389—
반응물Quino(2,3-b)acridine-7,14-dione, 5,6,12,13-tetrahydro-HCID 79973—
용매MethanolHCID 887—
생성물QuinacridoneHCID 13976—

반응 단계

79 Parts of methanol and 12 parts of a 50% NaOH aqeuous solution were fully stirred in a flask of stainless steel. 10 Parts of the 6,13-dihydroquinacridone obtained in Example 9 and 10 parts of sodium m-nitrobenzenesulfonate were gradually added, and the mixture was refluxed at 70° to 75° C. for 3 to 5 hours. The mixture was cooled until it had a temperature of 40° C. or lower, and the mixture was filtered. The resultant cake was washed with hot water until the wash water was colorless and transparent, and dried, to give 9.78 parts (98.4% of the theoretical yield) of an unsubstituted quinacridone. The quinacridone was measured for a purity by IR and absorbance to show 99.2% of quinacridone and 0.8% of 6,13-dihydroquinacridone. The quinacridone had a specific surface area of 22.8 m2 /g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05817817
출처 데이터셋uspto-grants-1998_10
ORD IDord-e943fda8c8104ec9adbfc0caeaa13b9e
출처 메모uspto-grants-1998_10