Sodium hydride → HCID 178425994, compound

HRID 1188270Notes

Reaction equation

HRID 1188270 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[C:5]=1[OH:16])([CH3:3])[CH3:2].[H-].[Na+].[Cl:19][Ti:20](Cl)([Cl:31])[C:21]1([CH3:30])[C:25]([CH3:26])=[C:24]([CH3:27])[C:23]([CH3:28])=[C:22]1[CH3:29]>C1(C)C=CC=CC=1>[Cl:19][Ti:20]([Cl:31])([C:21]1([CH3:30])[C:22]([CH3:29])=[C:23]([CH3:28])[C:24]([CH3:27])=[C:25]1[CH3:26])[O:16][C:5]1[C:6]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:7][CH:8]=[CH:9][C:4]=1[CH:1]([CH3:3])[CH3:2]

Participants

5

Procedure

700 mg (3.28 mmol) of 2-isopropyl-6-phenylphenol and 236 mg (9.84 mmol) of sodium hydride were dissolved in 10 ml of toluene, and then refluxed for 4 hours. The refluxed solution was cooled to room temperature, and then a solution of 930 mg (3.21 mmol) of trichloro(pentamethylcyclopentadienyl)titanium (IV) was slowly added dropwise thereto, and the mixture was refluxed for 24 hours. After completion of the reflux reaction, volatile components were removed from the reaction solution, and the residue was washed with purified hexane, recrytallized from a mixed solvent of toluene/hexane −35° C., filtered, and then dried in a vacuum, thus obtaining 1.0 g of a red solid.

Workup

  1. temperaturerefluxed for 4 hours
  2. temperaturethe mixture was refluxed for 24 hours
  3. customAfter completion of the reflux reaction, volatile components
  4. customwere removed from the reaction solution
  5. washthe residue was washed with purified hexane
  6. customrecrytallized from a mixed solvent of toluene/hexane −35° C.
  7. filtrationfiltered
  8. customdried in a vacuum

Sources & evidence

ORD record
ord-57116192ed924286b2702619b025267e
Source dataset
uspto-grants-2014_03
Patent number
US08674026B2

Reaction notes

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