Hydrogen Sulfide → Anthraquinone

HRID 1380218

반응식

HRID 1380218 반응식
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

참가 물질

4

반응물 2

HCID 402Hydrogen Sulfide2회HCID 142749441-tert-Butylanthracene-9,10-dione

생성물 2

HCID 6780AnthraquinoneHCID 210829,10-Anthracenediol

실험 절차

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.

출처 및 근거

ORD 기록
ord-f19aadf040314c9c9843f27d8b6328fe
출처 데이터셋
uspto-grants-1986_04
특허 번호
US04581128

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