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

HRID 127767ノート

反応式

HRID 127767 の反応式
[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]

参加物

6

反応条件

温度
-20 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-59fabc5f63e447d3856c5ecd3af6ddf6
出典データセット
uspto-grants-1981_03
特許番号
US04256878

反応ノート

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