Hydrogen Sulfide → Anthraquinone

HRID 1981474

반응식

HRID 1981474 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-8b99a374a52d4912b8f4a1b042f58312
출처 데이터셋
uspto-grants-1986_06
특허 번호
US04592905

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