Diethyl Ether → 63826-91-5

HRID 460982Notes

Reaction equation

HRID 460982 reaction equation
Br[C:2]1[S:3][C:4]([CH3:9])=[C:5]([Br:8])[C:6]=1[CH3:7].C[CH2:11][O:12]CC.C([Li])CCC>CN(C)C=O>[Br:8][C:5]1[C:6]([CH3:7])=[C:2]([CH:11]=[O:12])[S:3][C:4]=1[CH3:9]

Participants

5

Conditions

Temperature
-35 °C

Procedure

15.0 G. of 2,4-dibromo-3,5-dimethylthiophene was dissolved in 250 ml. of anhydrous ether and cooled to -70° C. with stirring under argon. 24 Ml. of a 2.4 M solution of n-butyl lithium was slowly added to the solution and the mixture was warmed to -35° C. for 10 minutes, and then cooled again to -70° C. 7.3 G. of dimethylformamide was added slowly to the mixture and the reaction mixture was warmed to room temperature for 14 hours. The resulting solution was poured into ice water, stirred for 20 minutes and extracted with ethyl ether. The ether extracts were combined, washed with an aqueous solution of 5% sodium carbonate, saturated sodium chloride solution, dried with sodium sulfate, filtered and evaporated to yield 4-bromo-3,5-dimethylthiophene-2-carboxaldehyde, m.p. 44°-45° C.

Workup

  1. temperaturecooled again to -70° C
  2. temperaturethe reaction mixture was warmed to room temperature for 14 hours
  3. stirringstirred for 20 minutes
  4. extractionextracted with ethyl ether
  5. washwashed with an aqueous solution of 5% sodium carbonate, saturated sodium chloride solution
  6. dry with materialdried with sodium sulfate
  7. filtrationfiltered
  8. customevaporated

Sources & evidence

ORD record
ord-9c61a388daf34417b935d6110d8292d1
Source dataset
uspto-grants-1977_12
Patent number
US04061656

Reaction notes

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