1-(3,5-Difluorophenyl)-4-pentylcyclohexan-1-OL → (4-Pentyl-1-cyclohexenyl)-3,5-difluorobenzene
反応式
O[C:2]1([C:13]2[CH:18]=[C:17]([F:19])[CH:16]=[C:15]([F:20])[CH:14]=2)[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[CH2:4][CH2:3]1>C1(C)C=CC=CC=1>[CH2:8]([CH:5]1[CH2:6][CH2:7][C:2]([C:13]2[CH:14]=[C:15]([F:20])[CH:16]=[C:17]([F:19])[CH:18]=2)=[CH:3][CH2:4]1)[CH2:9][CH2:10][CH2:11][CH3:12]参加物
3
実験手順
Mixture of (1-hydroxy-4-pentylcyclohexyl)-3,5-difluorobenzene (300 mmol), the Amberlist 15E (4.0 g), and 1,000 ml of toluene was refluxed for 6 hours. After allowed to cool, the Amberlist 15E was filtered off, the solvent was distilled off, and the residue was purified by column chromatography (eluent: heptane) to give a (4-pentyl-1-cyclohexenyl)-3,5-difluorobenzene (170 mmol).
後処理
- temperatureto cool
- filtrationthe Amberlist 15E was filtered off
- distillationthe solvent was distilled off
- customthe residue was purified by column chromatography (eluent: heptane)
出典と根拠
- ORDレコード
- ord-80cb0e6b77364f528f14b33ed4662b8f
- 出典データセット
- uspto-grants-2001_01
- 特許番号
- US06174458B1
反応ノート
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