3-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]Benzaldehyde → 3-(6-Chloro-1,3-benzthiazin-2-yl-transethenyl)benzyl alcohol t-butyldimethylsilyl ether
反応式
[CH3:1][CH:2]1[N:7]=[CH:6][C:5]2[CH:8]=[C:9]([Cl:12])[CH:10]=[CH:11][C:4]=2[S:3]1.[Si:13]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([CH:28]=O)[CH:23]=1)([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14]>N1CCCCC1.C1C=CC=CC=1.C(OCC)(=O)C>[Si:13]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24](/[CH:28]=[CH:1]/[CH:2]2[N:7]=[CH:6][C:5]3[CH:8]=[C:9]([Cl:12])[CH:10]=[CH:11][C:4]=3[S:3]2)[CH:23]=1)([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:14])[CH3:15]参加物
6
反応物 2
生成物 1
試薬・触媒・溶媒 3
実験手順
A mixture of 1.08 g of 2-methyl-6-chloro-1,3-benzthiazine 1.51 g of 3-formylbenzyl alcohol t-butyldimethylsilyl ether and 5 drops of piperidine in 60 ml of benzene was heated to reflux in a Dean-Stark trap for 1 hour. An additional 5 drops of piperidine were added and the refluxing continued from 30 hours. The mixture was diluted with 400 ml of ethyl acetate and washed with water (1×40 ml) and brine (1×40 ml). The organic layer was dried over magnesium sulfate and concentrated to 2 g of crude product which was chromatographed on silica gel using 5% ethyl acetate in hexane (v:v), 188 mg, m.p. 58°-60° C.
後処理
- temperaturewas heated
- temperatureto reflux in a Dean-Stark trap for 1 hour
- washwashed with water (1×40 ml) and brine (1×40 ml)
- dry with materialThe organic layer was dried over magnesium sulfate
- concentrationconcentrated to 2 g of crude product which
- customwas chromatographed on silica gel using 5% ethyl acetate in hexane (v:v), 188 mg, m.p. 58°-60° C.
出典と根拠
- ORDレコード
- ord-0249f3a74d674c23a26e9afe34fe8653
- 出典データセット
- uspto-grants-1994_06
- 特許番号
- US05322847
反応ノート
読み込み中…