反応式
[CH2:1]([O:5][C:6]1[CH:7]=[C:8]([OH:12])[CH:9]=[CH:10][CH:11]=1)[CH2:2][CH2:3][CH3:4].[Br:13][CH2:14][CH2:15]Br>>[Br:13][CH2:14][CH2:15][O:12][C:8]1[CH:9]=[CH:10][CH:11]=[C:6]([O:5][CH2:1][CH2:2][CH2:3][CH3:4])[CH:7]=1参加物
3
実験手順
Prepared analogously to the method described in Example D above from 3-(n-butoxy)phenol (16.6 g; 0.1 mol; from Example B above) and 1,2-dibromoethane (100 ml; 1.16 mol). Following work up, the residue was chromatographed on silica gel with diisopropyl ether as eluent. The resultant oil was distilled to to yield 23.1 g (85%) of the title compound as an oil which subsequently crystallised (98% purity). bp 105-108° C. (0.01 mm Hg) mp 32-34° C. MW=273 (GC-MS)
後処理
- customPrepared analogously to the method
- customthe residue was chromatographed on silica gel with diisopropyl ether as eluent
- distillationThe resultant oil was distilled
出典と根拠
- ORDレコード
- ord-e67e2d960c254f80ab0e57522fcde1e6
- 出典データセット
- uspto-grants-2001_10
- 特許番号
- US06310252B1
関連ノート
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