Cyclohexane, (bromomethyl)- → 3-(Cyclohexylmethoxy)-5-methylphenol

HRID 1014653Notes

Reaction equation

HRID 1014653 reaction equation
[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

Participants

5

Reactant 3

HCID 137636Cyclohexane, (bromomethyl)-HCID 3083941Resorcinol, 5-methyl-, monohydrateHCID 23665647Potassium tert-butoxide

Product 1

HCID 230943513-(Cyclohexylmethoxy)-5-methylphenol

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
60 °C

Procedure

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).

Workup

  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)

Sources & evidence

ORD record
ord-16c11ce085ba48e1ad5693f4fa3c9e9b
Source dataset
uspto-grants-2011_07
Patent number
US07982071B2

Reaction notes

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