Sulfuric Acid → 4-Fluoro-2-(1-methylcyclohexyl)phenol

HRID 383413

反応式

HRID 383413 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[CH3:9][C:10]1(O)[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1.S(=O)(=O)(O)O>C(Cl)Cl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([C:10]2([CH3:9])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]2)[CH:3]=1

参加物

5

反応物 3

HCID 1118Sulfuric AcidHCID 97324-FluorophenolHCID 115501-Methylcyclohexanol

生成物 1

HCID 593949974-Fluoro-2-(1-methylcyclohexyl)phenol

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

4-Fluorophenol (41.8 g, 373 mmol) and 1-methylcyclohexanol (63.8 g, 560 mmol) dissolved in 600 mL of dried CH2Cl2, were treated with concentrated sulfuric acid (98%, 22.3 mL, 418 mmol). The mixture was stirred at room temperature for 50 hours. The reaction mixture was then extracted by CH2Cl2 (250 mLx3). The organic layer was washed with saturated a.q NaHCO3., dried over MgSO4, and evaporated under vacuum. The residue was purified by column chromatography on silica gel to give 4-fluoro-2-(1-methylcyclohexyl)phenol as a dark green oil—47.6 g. 1H NMR (400 MHz, CDCl3) δ 7.00 (dd, J=3.2, 11.2 Hz, 1H), 6.76-6.71 (m, 1H), 6.62-6.59 (m, 1H), 5.27 (brs, 1H), 2.13-2.07 (M, 2H), 1.70-1.37 (m, 8H), 1.32 (s, 3H).

後処理

  1. extractionThe reaction mixture was then extracted by CH2Cl2 (250 mLx3)
  2. washThe organic layer was washed with saturated a.q NaHCO3
  3. dry with material, dried over MgSO4
  4. customevaporated under vacuum
  5. customThe residue was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-03f96806035348698365e249e47fb222
出典データセット
uspto-grants-2013_02
特許番号
US08367660B2

関連ノート

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