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Diethyl Ether → 2,4-Dimethylthiophene-3-carbaldehyde

HRID 1764579
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HRID 1764579 반응식
[CH3:1][C:2]1[S:3][CH:4]=[C:5]([CH3:8])[C:6]=1Br.C[CH2:10][O:11]CC.C([Li])CCC.CN(C)C=O>CCCCCC>[CH3:1][C:2]1[S:3][CH:4]=[C:5]([CH3:8])[C:6]=1[CH:10]=[O:11]
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참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 6228DimethylformamideHCID 106317743-Bromo-2,4-dimethylthiopheneHCID 178418339Butyllithium

생성물 1

HCID 111477702,4-Dimethylthiophene-3-carbaldehyde

시약·촉매·용매 1

HCID 8058Hexane용매

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온도
-20 °C

실험 절차

A solution of 15 g. (79.0 mmol) of 2,4-dimethyl-3-bromothiophene in 120 ml. of dry ether was cooled to -70° C. and 36 ml. of a hexane solution of n-butyl lithium (2.4 molar, 86.4 mmol) were added dropwise. The reaction mixture was allowed to warm up to -20° C. for 10 min., cooled again to -70° C. and then quenched by adding dropwise 15 g. (0.205 mol) of dimethylformamide. The mixture was stirred at room temperature overnight, poured into ice water, stirred for 15 min. and extracted four times with ether. The ether phase was washed with saturated sodium chloride solution, dried and evaporated. The resulting oily residue was distilled to yield 2,4-dimethylthiophene-3-carboxaldehyde, b.p. 50°-55° C./0.1 mm.

후처리

  1. temperaturecooled again to -70° C.
  2. customquenched
  3. additionby adding dropwise 15 g
  4. stirringstirred for 15 min.
  5. extractionextracted four times with ether
  6. washThe ether phase was washed with saturated sodium chloride solution
  7. customdried
  8. customevaporated
  9. distillationThe resulting oily residue was distilled

출처 및 근거

ORD 기록
ord-52a7df71499f46b4831950f14549fca8
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04116975

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