Ethylene carbonate → HCID 22036399, compound

HRID 1789711Notes

Reaction equation

HRID 1789711 reaction equation
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[OH:9].C([O-])([O-])=O.[K+].[K+].C1(=O)O[CH2:21][CH2:20][O:19]1>CN(C=O)C>[F:1][C:2]([F:10])([F:11])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][CH2:21][CH2:20][OH:19]

Participants

5

Conditions

Temperature
150 °C

Procedure

A mixture of 2-trifluoromethylphenol (2.00 g, 12.3 mmol), K2CO3 (1.71 g, 12.3 mmol) and ethylene carbonate (1.20 g, 13.6 mmol) in dry DMF (30 mL) was heated at 150° C. for 1 h. After cooling, the reaction was quenched by addition of water (10 mL). The mixture was concentrated in vacuo and the residue partitioned between water (30 mL) and EtOAc (30 mL). The aqueous phase was extracted with additional portions of EtOAc (3×30 mL). The combined organic layers were treated with charcoal, dried over MgSO4, and filtered through Celite. The filtrate was concentrated in vacuo and the remaining oil was purified by chromatography on silica gel using n-hexane/EtOAc (80:20) as eluent to give 0.50 g (20%) of the title product as white crystals: mp 74-77° C. Anal. (C9H9F3O2) C, H.

Workup

  1. temperatureAfter cooling
  2. customthe reaction was quenched by addition of water (10 mL)
  3. concentrationThe mixture was concentrated in vacuo
  4. customthe residue partitioned between water (30 mL) and EtOAc (30 mL)
  5. extractionThe aqueous phase was extracted with additional portions of EtOAc (3×30 mL)
  6. additionThe combined organic layers were treated with charcoal
  7. dry with materialdried over MgSO4
  8. filtrationfiltered through Celite
  9. concentrationThe filtrate was concentrated in vacuo
  10. customthe remaining oil was purified by chromatography on silica gel

Sources & evidence

ORD record
ord-210ae9ffb2e041219ef55f98f29082f9
Source dataset
uspto-grants-2006_07
Patent number
US07071180B2

Reaction notes

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