1-Chloro-4-hydroxyanthraquinone → 1-Hydroxyanthraquinone

HRID 256277

반응식

HRID 256277 반응식
Cl[C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[C:5]([OH:18])=[CH:4][CH:3]=1.C1(C2C=CC(N)=CC=2)CCCCC1.C([O-])(=O)C.[Na+]>[N+](C1C=CC=CC=1)([O-])=O.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[OH:18][C:5]1[C:6]2[C:7](=[O:17])[C:8]3[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=3)[C:14](=[O:16])[C:15]=2[CH:2]=[CH:3][CH:4]=1

참가 물질

6

실험 절차

The pleochroic dye 1-cyclohexylphenylamino, 4-hydroxyanthraquinone was prepared by combining equimolar quantities of 1-chloro-4-hydroxy anthraquinone and 4-cyclohexylaniline and heating in the presence of a catalytic amount of copper acetate (0.1 g/0.1 mole) and sodium acetate (10 g/0.1 mole) in nitrobenzene. The reaction was run and the dye separated and tested as in Example 70. The dye had an absorption maxima at 594 nm and an optical order parameter of 0.75.

후처리

  1. customthe dye separated

출처 및 근거

ORD 기록
ord-4036e1c133394fe891b76e93ce871235
출처 데이터셋
uspto-grants-1987_10
특허 번호
US04702561

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