反応式
[F:1][C:2]1[C:3](=O)[C:4]2[C:12](=[CH:13][CH:14]=1)[C:11]1[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=1)[CH:5]=2.[C:16]1([Li])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.C1C[O:26]CC1>C1CCCCC1.CCOCC>[F:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)([OH:26])[C:4]=2[CH:3]=1参加物
5
実験手順
To a stirred, ice-cooled solution of 2-fluorofluorenone (2.0 g, 10 mmol) in 15 mL of dry THF under N2 was added 10 mL of 2.4 M phenyllithium solution in cyclohexane-Et2O (7:3), keeping T<20° C. The mixture was quenched with water and the product isolated with EtOAc and purified by flash chromatography (7% EtOAc-hexanes) to give 2.52 g (90%) of 2-fluoro-9-phenylfluoren-9-ol.
後処理
- customT<20° C
- customThe mixture was quenched with water
- customthe product isolated with EtOAc
- custompurified by flash chromatography (7% EtOAc-hexanes)
出典と根拠
- ORDレコード
- ord-28b14d14aa0040648ba12bf59967ae09
- 出典データセット
- uspto-grants-2001_01
- 特許番号
- US06177427B1
関連ノート
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