Ethylene Glycol → HCID 59545167, compound

HRID 1892879Notes

Reaction equation

HRID 1892879 reaction equation
Cl[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[C:9](=[O:11])[CH:8]([CH2:12][CH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)[CH2:7]2.C[C:20]1[C:25]([CH3:26])=[CH:24][CH:23]=[CH:22][C:21]=1B(O)O.[C:30](=O)([O-])[O-].[Na+].[Na+].C(O)CO>O>[CH3:26][C:25]1[CH:24]=[C:23]([C:2]2[CH:3]=[CH:4][CH:5]=[C:6]3[C:10]=2[C:9](=[O:11])[CH:8]([CH2:12][CH:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)[CH2:7]3)[CH:22]=[C:21]([CH3:30])[CH:20]=1

Participants

6

Reactant 4

HCID 174Ethylene GlycolHCID 10340Sodium CarbonateHCID 27733952,3-Dimethylphenylboronic acidHCID 58444101HCID 58444101, compound

Product 1

HCID 59545167HCID 59545167, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
125 °C

Procedure

20 g (76 mmole) 7-Chloro-2-cyclohexylmethyl-indan-1-one, 13.7 g (1.2 eq.) 2,3-dimethylphenyl boronic acid, 17.75 g sodium carbonate, 250 ml ethylene glycol and 50 ml water were placed in a 1 l—roundbottom flask equipped with a mechanical stirrer and a reflux condenser. The mixture was degassed three times by slight evacuation and recharging with argon. A premixed catalyst solution consisting of 34 mg (0.2 mole %) palladium acetate, 1 ml NaTPPTS (2.6 M in water, 0.8 mole %) and 2 ml of water was added and the mixture was refluxed at 125° C. until complete conversion (approx. 4 h). 100 ml of water were added and the mixture was extracted three times with 100 ml of toluene each. The combined organic layers were washed twice with 100 ml water and once with 100 ml of a saturated sodium chloride solution. Drying over magnesium sulphate and evaporation of the solvent in vacuo yielded 27.7 g (quant.) of the desired product as a yellow sticky oil. 1H-NMR (400 MHz, CDCl3): δ=7.55 (t, 1H, aromatic), 7.39 (d, 1H, aromatic), 7.28-7.02 (m, 3H, aromatic), 3.34 (m, 1H, (C═O)CH), 2.81-2.69 (m, 2H, benzylic), 2.37 (s, 6H, Ph-CH3), 1.89-0.89 (m, 10H, aliphatic) ppm.

Workup

  1. customequipped with a mechanical stirrer and a reflux condenser
  2. customThe mixture was degassed three times by slight evacuation
  3. additionwas added
  4. addition100 ml of water were added
  5. extractionthe mixture was extracted three times with 100 ml of toluene each
  6. washThe combined organic layers were washed twice with 100 ml water and once with 100 ml of a saturated sodium chloride solution
  7. dry with materialDrying over magnesium sulphate and evaporation of the solvent in vacuo

Sources & evidence

ORD record
ord-86f93c0711c74f92b8caacea45a54155
Source dataset
uspto-grants-2013_08
Patent number
US08507706B2

Reaction notes

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