Benzyl Alcohol → Dibenzyl ether

HRID 1611465Notes

Reaction equation

HRID 1611465 reaction equation
[CH2:1]([OH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[K+].[CH2:11]1O[CH:12]1[CH3:13].S(=O)(=O)(O)O>>[CH2:1]([O:8][CH2:13][C:12]1[CH:11]=[CH:4][CH:3]=[CH:2][CH:1]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Conditions

Temperature
110 °C

Procedure

2297.75 g (21.24 moles) of benzyl alcohol was placed in a dry, stirred pressure vessel fitted with a nitrogen inlet. A catalytic amount (6 g) of KOH was added as a 40% aqueous solution. The vessel was purged with nitrogen and heated to 110° C. Vacuum was applied for 1 hour to remove the water vapors from the headspace of the vessel, and the mixture was further heated to 130° C. After 3702.25 g (63.74 moles) of propylene oxide were added, the reaction mixture was stirred for additional 3 hours to complete the reaction. The progress of the reaction was monitored by the uptake of the reagent and the measurement of the pressure in the vessel. The reaction mixture was cooled to 110° C., and a vacuum was applied for approximately 1 hour. To neutralize KOH in the reaction mixture, 29 g of 25% sulfuric acid was added. The mixture was stirred for 10 minutes, and the pH was adjusted to 5.7. Upon cooling, PPG-3 Benzyl Ether, a thin light yellow liquid, was isolated as the major product.

Workup

  1. customfitted with a nitrogen inlet
  2. customThe vessel was purged with nitrogen
  3. customto remove the water vapors from the headspace of the vessel
  4. temperaturethe mixture was further heated to 130° C
  5. stirringthe reaction mixture was stirred for additional 3 hours
  6. customthe reaction
  7. temperatureThe reaction mixture was cooled to 110° C.
  8. waita vacuum was applied for approximately 1 hour
  9. additionwas added
  10. stirringThe mixture was stirred for 10 minutes
  11. temperatureUpon cooling

Sources & evidence

ORD record
ord-ec8dfba0a9774d90a207bcebf45902e4
Source dataset
uspto-grants-2006_01
Patent number
US06987195B2

Reaction notes

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