反応式
O[CH:2]1[CH2:11][CH2:10][CH2:9][C:8]2[N:7]=[CH:6][CH:5]=[CH:4][C:3]1=2.[Cl-:12]>>[Cl:12][CH:2]1[CH2:11][CH2:10][CH2:9][C:8]2[N:7]=[CH:6][CH:5]=[CH:4][C:3]1=2参加物
3
実験手順
5-Hydroxy-5,6,7,8-tetrahydroquinoline from step 1 above was converted to the chloride using the procedure as given in step 2 of Example 3. The crude 5-chloro-5,6,7,8-tetrahydroquinoline was purified by pressurized silica gel column chromatography using 7:3 EtOAc:hexane as eluant. 5-Chloro-5,6,7,8-tetrahydroquinoline was obtained as a pale yellow oil (TLC Rf = 0.40 (8:2 EtOAc:hexane)).
後処理
- customThe crude 5-chloro-5,6,7,8-tetrahydroquinoline was purified by pressurized silica gel column chromatography
出典と根拠
- ORDレコード
- ord-f398a21cbf54472fb39850596842c269
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05756497
関連ノート
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