참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Sodium 3-nitrobenzenesulfonate | HCID 31389 | — |
| 반응물 | Quino(2,3-b)acridine-7,14-dione, 5,6,12,13-tetrahydro- | HCID 79973 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Quinacridone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05817817 |
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| 출처 데이터셋 | uspto-grants-1998_10 |
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| ORD ID | ord-e943fda8c8104ec9adbfc0caeaa13b9e |
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| 출처 메모 | uspto-grants-1998_10 |
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