Water → 3-(Cyclohexylmethoxy)-5-methylphenol

HRID 74408

反応式

HRID 74408 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([OH:8])[CH:7]=1.O.CC(C)([O-])C.[K+].Br[CH2:18][CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1>CN(C=O)C>[CH:19]1([CH2:18][O:8][C:6]2[CH:5]=[C:4]([OH:9])[CH:3]=[C:2]([CH3:1])[CH:7]=2)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1

参加物

6

反応条件

温度
60 °C

実験手順

To a solution of 5-methylbenzene-1,3-diol.H2O (1.0 g, 7.0 mmol) in DMF (15 ml) was added potassium tert-butoxide (0.86 g, 77 mmol). The mixture was stirred at 60° C. for 1 h. To the mixture was added (bromomethyl)cyclohexane (1.2 g, 7.0 mmol). The reaction mixture was stirred at 60° C. for 18 h, concentrated under vacuum, partitioned between water (40 ml) and ethyl acetate (60 ml). Ethyl acetate portion was dried over Na2SO4. Purification by chromatography (10 to 30% EtOAc-hexanes gradient) gave 3-(cyclohexylmethoxy)-5-methylphenol (133) as a light yellow solid. Yield (0.40 g, 26%): 1H NMR (400 MHz, CDCl3) δ 6.31 (s, 1H), 6.20-6.22 (m, 2H), 4.62 (bs, 1H), 3.69 (d, J=6.4 Hz, 2H), 2.50 (s, 3H), 1.64-1.88 (m, 6H), 1.16-1.34 (m, 3H), 0.98-1.08 (m, 2H).

後処理

  1. stirringThe reaction mixture was stirred at 60° C. for 18 h
  2. concentrationconcentrated under vacuum
  3. custompartitioned between water (40 ml) and ethyl acetate (60 ml)
  4. dry with materialEthyl acetate portion was dried over Na2SO4
  5. customPurification by chromatography (10 to 30% EtOAc-hexanes gradient)

出典と根拠

ORDレコード
ord-81c7e6e90b6240fc8c95e26ceeb9628f
出典データセット
uspto-grants-2014_09
特許番号
US08829244B2

関連ノート

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