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Diethyl Ether → 4-Bromo-3,5-dimethylthiophene-2-carbaldehyde

HRID 904476
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HRID 904476 반응식
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]
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참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 105880762,4-Dibromo-3,5-dimethylthiopheneHCID 178418339Butyllithium

생성물 1

HCID 128752694-Bromo-3,5-dimethylthiophene-2-carbaldehyde

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
-35 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-55bffb4672a94c2d9f2a5483a54753cc
출처 데이터셋
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04230872

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