Tetrahydrofuran → HCID 19759295、化合物

HRID 1586824ノート

反応式

HRID 1586824 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]3[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=3[CH:9]=2)=[CH:4][CH:3]=1.[O:17]1CCC[CH2:18]1.C([Li])CCC>CN(C)C=O>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]3[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=3[C:9]=2[CH:18]=[O:17])=[CH:4][CH:3]=1

参加物

5

反応条件

温度
-78 °C

実験手順

To a solution of 2-(4-methylphenyl)benzo[b]thiophene (896 mg) in freshly distillated tetrahydrofuran (15 ml) was added n-butyllithium (2.75 ml, 1.6 mol solution in n-hexane) through a syringe at -78° C. The solution was stirred at -78° C. for 10 minutes and then at ambient temperature for half an hour. To the deep red colored solution was added N,N-dimethylformamide (365mg) at 5° C. The mixture was stirred at ambient temperature for one hour, quenched with aqueous saturated ammonium chloride solution, and extracted with diethyl ether. The organic layer was washed with aqueous saturated ammonium chloride solution, dried, and concentrated in vacuo to give a yellow residue, which was purified by flash column chromatography on silica gel eluted with 50% n-hexane in dichloromethane to yield 2-(4-methylphenyl)benzo[b]thiophene-3-carbaldehyde (285 mg) as white crystals.

後処理

  1. waitat ambient temperature for half an hour
  2. stirringThe mixture was stirred at ambient temperature for one hour
  3. customquenched with aqueous saturated ammonium chloride solution
  4. extractionextracted with diethyl ether
  5. washThe organic layer was washed with aqueous saturated ammonium chloride solution
  6. customdried
  7. concentrationconcentrated in vacuo
  8. customto give a yellow residue, which
  9. customwas purified by flash column chromatography on silica gel
  10. washeluted with 50% n-hexane in dichloromethane

出典と根拠

ORDレコード
ord-19ab70f4917b4ca7a518ef753b060680
出典データセット
uspto-grants-1993_06
特許番号
US05215994

反応ノート

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