반응식
S([O-])([O-])=O.C1C(C(N)=O)=CN(C2OC(COP(OP(OCC3OC(N4C5N=CN=C(N)C=5N=C4)C(OP([O-])([O-])=O)C3O)([O-])=O)([O-])=O)C(O)C2O)C=C1.[Na+:53].[Na+:54].[Na+].[Na+].[C:57]1([C:76]([OH:78])=[O:77])[C:66]2[C:65]([C:67]([OH:69])=[O:68])=[CH:64][CH:63]=[C:62]([C:70]([OH:72])=[O:71])[C:61]=2[C:60]([C:73]([OH:75])=[O:74])=[CH:59][CH:58]=1>>[Na:53][Na:54].[C:57]1([C:76]([OH:78])=[O:77])[C:66]2[C:65]([C:67]([OH:69])=[O:68])=[CH:64][CH:63]=[C:62]([C:70]([OH:72])=[O:71])[C:61]=2[C:60]([C:73]([OH:75])=[O:74])=[CH:59][CH:58]=1참가 물질
반응물 3
생성물 2
실험 절차
The process as claimed in claim 6, wherein, after the oxidation has ended the reaction mixture is subjected to a heat treatment at a temperature of between 90° and 120° C. under the autogenous pressure of 1 to 10 bar which is established, in the presence of sulfite, the resulting suspension of the tetrasodium salt of naphthalene-1,4,5,8-tetracarboxylic acid is cooled, after the reaction vessel has been let down, to a temperature of below 40° C. the pH is then adjusted to 4.5 to 5 by acidification, the resulting disodium salt of naphthalene-1,4,5,8-tetracarboxylic acid is isolated, this salt is converted into the tetrasodium salt of naphthalene-1,4,5,8-tetracarboxylic acid in an aqueous alkali metal hydroxide solution and, optionally after removal of insoluble impurities, naphthalene-1,4,5,8-tetracarboxylic acid 1,8-monoanhydride is precipitated by acidification to a pH of less than 2 at a temperature of 80° to 100° C.
후처리
- customis subjected to a heat treatment at a temperature of between 90° and 120° C. under the autogenous pressure of 1 to 10 bar which
- temperatureis cooled
- customhas been let down, to a temperature of below 40° C.
출처 및 근거
- ORD 기록
- ord-fd16b247f4bd4348a18179488e19f6c6
- 출처 데이터셋
- uspto-grants-1993_10
- 특허 번호
- US05254796
연결된 노트
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