Dimethylformamide → 1-Ethoxymethoxy-4-pentafluoroethyl benzene

HRID 2094458Notes

Reaction equation

HRID 2094458 reaction equation
[CH2:1]([O:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9](I)=[CH:8][CH:7]=1)[CH3:2].[F:13][C:14]([F:22])([F:21])[C:15]([F:20])([F:19])C([O-])=O.[Na+].CN(C=O)C>[Cu]I.C1(C)C=CC=CC=1>[CH2:1]([O:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:15]([F:20])([F:19])[C:14]([F:22])([F:21])[F:13])=[CH:8][CH:7]=1)[CH3:2]

Participants

6

Conditions

Temperature
145 °C

Procedure

A mixture of 7.5 g of crude product of 1-ethoxymethoxy-4-iodobenzene, 10.0 g of sodium pentafluoropropionate salt, 10.27 g of copper(I) iodide, 120 ml of DMF and 45 ml of toluene was stirred while heating at 140 to 150° C. for one hour to remove about 40 ml of toluene. The reaction mixture was heated to reflux at 160 to 170° C. for further five hours, and then cooled to room temperature and poured into ice water. To the reaction mixture, 200 ml of diethyl ether was added. The reaction mixture was filtered through Celite™. The filtrate was extracted with diethyl ether. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give 5.45 g of 1-ethoxymethoxy-4-pentafluoroethyl benzene.

Workup

  1. customto remove about 40 ml of toluene
  2. temperatureThe reaction mixture was heated
  3. temperatureto reflux at 160 to 170° C. for further five hours
  4. temperaturecooled to room temperature
  5. additionpoured into ice water
  6. additionTo the reaction mixture, 200 ml of diethyl ether was added
  7. filtrationThe reaction mixture was filtered through Celite™
  8. extractionThe filtrate was extracted with diethyl ether
  9. washThe combined organic layers were washed with water
  10. dry with materiala saturated sodium chloride solution, dried over anhydrous magnesium sulfate
  11. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-2575519bb6de47a5a82bf5dc415b7eeb
Source dataset
uspto-grants-2013_05
Patent number
US08445522B2

Reaction notes

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