Hydrogen Sulfide → 蒽醌

HRID 1380218

反应方程式

HRID 1380218 反应方程式
S.C([C:6]1[C:19]2[C:18](=[O:20])[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11](=[O:21])[C:10]=2[CH:9]=[CH:8][CH:7]=1)(C)(C)C>>[CH:13]1[C:12]2[C:11](=[O:21])[C:10]3[C:19](=[CH:6][CH:7]=[CH:8][CH:9]=3)[C:18](=[O:20])[C:17]=2[CH:16]=[CH:15][CH:14]=1.[CH:15]1[CH:16]=[C:17]2[C:18]([OH:20])=[C:19]3[C:10](=[C:11]([OH:21])[C:12]2=[CH:13][CH:14]=1)[CH:9]=[CH:8][CH:7]=[CH:6]3

参与物

4

反应物 2

HCID 402Hydrogen Sulfide2 次HCID 142749441-tert-Butylanthracene-9,10-dione

产物 2

HCID 6780蒽醌HCID 21082蒽-9,10-二醇

实验过程

H2S and t-butyl anthraquinone are dissolved in several solvents. They are then reacted in the H2S reactor at optimum conditions to determine which combination of reactants and solvents yields the greatest conversion of anthraquinone to anthrahydroquinone. The results are set forth in Table 1 below.

来源与证据

ORD记录
ord-f19aadf040314c9c9843f27d8b6328fe
来源数据集
uspto-grants-1986_04
专利号
US04581128

关联笔记

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