(3,4-Dihydro-2H-1-thia-4a,9-diaza-fluoren-6-yl)-methanol → 3,4-Dihydro-2H-1-thia-4a,9-diaza-fluorene-6-carbaldehyde
反応式
[S:1]1[C:13]2[N:5]([C:6]3[C:11]([N:12]=2)=[CH:10][CH:9]=[C:8]([CH2:14][OH:15])[CH:7]=3)[CH2:4][CH2:3][CH2:2]1>[O-2].[O-2].[Mn+4].C(Cl)(Cl)Cl>[S:1]1[C:13]2[N:5]([C:6]3[C:11]([N:12]=2)=[CH:10][CH:9]=[C:8]([CH:14]=[O:15])[CH:7]=3)[CH2:4][CH2:3][CH2:2]1参加物
4
実験手順
To a round bottomed flask was loaded 1.1 grams of (3,4-Dihydro-2H-1-thia-4a,9-diaza-fluoren-6-yl)-methanol, 6 grams of manganese dioxide and 250 ml chloroform. The mixture was stirred for one hour at room temperature and then filtered through a pad of celite. This yielded 0.67 grams of product (61%). MS: 219.0 (M+H). H-NMR(CDCl3): δ 10.04(s, 1H), 7.67 (m, 3H), 4.25 (m, 2H), 3.27(m, 2H), 2.50 (m, 2H).
後処理
- customTo a round bottomed flask was loaded
- filtrationfiltered through a pad of celite
出典と根拠
- ORDレコード
- ord-feccae0f46d54673a78ea4794791f36f
- 出典データセット
- uspto-grants-2006_03
- 特許番号
- US07018997B2
反応ノート
読み込み中…