Trifluoroacetic acid → 5,6-Dihydroxyindole
反応式
C([O:8][C:9]1[C:19]([O:20]CC2C=CC=CC=2)=[CH:18][C:12]([CH:13]=[CH:14][N+:15]([O-:17])=[O:16])=[C:11]([N+:28]([O-:30])=[O:29])[CH:10]=1)C1C=CC=CC=1.FC(F)(F)C(O)=O>>[OH:20][C:19]1[CH:18]=[C:12]2[C:11](=[CH:10][C:9]=1[OH:8])[NH:28][CH:14]=[CH:13]2.[OH:8][C:9]1[C:19]([OH:20])=[CH:18][C:12]([CH:13]=[CH:14][N+:15]([O-:17])=[O:16])=[C:11]([N+:28]([O-:30])=[O:29])[CH:10]=1参加物
4
実験手順
or by debenzylation of 4,5-dibenzyloxy-2,β-di-nitrostyrene; in this case the debenzylation is performed by means of trifluoroacetic acid. In a second stage 5,6-dihydroxyindole is obtained from 4,5-dihydroxy-2,β-di-nitrostyrene as indicated above (U.S. Pat. No. 4,595,765).
出典と根拠
- ORDレコード
- ord-8b59e298c5734d82a89c2b0a69d0d239
- 出典データセット
- uspto-grants-1996_03
- 特許番号
- US05498746
反応ノート
読み込み中…