참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sulfur Dioxide | HCID 1119 | — |
| 반응물 | 1,6-Cleve's acid | HCID 8408 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Phosphonic acid, P-(3-aminophenyl)- | HCID 79477 | — |
| 반응물 | Sodium Bisulfite | HCID 23665763 | — |
| 생성물 | 5-(3-Phosphonoanilino)naphthalene-2-sulfonic acid | HCID 21408081 | — |
반응 단계
Sodium bisulphite liquor (40% -- 23 parts), sodium hydroxide liquor (70° Tw -- 8.1 parts), salt (1.8 parts), 1-amino-6-sulphonaphtalene (11.2 parts) and 3-aminophenylphosphonic acid (10.4 parts) are heated in a sealed tube for 10 hours at 130° C. After cooling the tube is opened and hydrochloric acid (36% - 13.9 parts) is added until an acid reaction is obtained on Congo Red paper. The suspension is boiled under reflux for 1 hour until evolution of sulphur dioxide has essentially ceased. During this period samples are spotted on to Congo Red paper to confirm acid reaction. The suspension is cooled to room temperature and filtered. The filtrate is set stirring and sodium chloride (8 parts = 20% wt/vol) added. After stirring for 18 hours the suspension is filtered under vacuum and the cake pressed well to remove mothers liquor. The paste (8 parts) is dried in air at 50°-60° C to give 7 parts of 1-(3-phosphonophenylamino)-6-sulphonaphthalene.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04051175 |
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| 출처 데이터셋 | uspto-grants-1977_09 |
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| ORD ID | ord-2d05a617a8a2480e83c823609123cfe6 |
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| 출처 메모 | uspto-grants-1977_09 |
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