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Dimethylformamide → HCID 67273752、化合物

HRID 1696735
ノート
印刷プレビュー

反応式

HRID 1696735 の反応式
[S:1](=[O:4])(=O)=[O:2].C[N:6](C)C=O.[CH2:10]([C:14]1[S:15][CH:16]=[CH:17][C:18]=1[CH3:19])[CH:11]([CH3:13])[CH3:12].S(Cl)(Cl)=O>ClCCl>[CH2:10]([C:14]1[S:15][C:16]([S:1]([NH2:6])(=[O:4])=[O:2])=[CH:17][C:18]=1[CH3:19])[CH:11]([CH3:13])[CH3:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 24682Sulfur trioxideHCID 10241021HCID 10241021、化合物

生成物 1

HCID 67273752HCID 67273752、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
80 °C

実験手順

To a mixture of 0.368 g of the complex of sulfur trioxide with dimethylformamide in 1.5 ml dichloromethane was added 0.309 g 2-isobutyl-3-methyl-thiophene and the mixture was heated to 55° C. for 30 min. and to 80° C. for an other 30 min. The mixture was cooled to room temperature and 0.286 g thionylchloride was added. The mixture was heated to 55° C. for ca 30 min cooled to room temperature and poored onto ice and extracted with ethyl acetate, the phases were separated and the organic phase was washed with water and brine and evaporated. The residue was taken up in 10 ml acetone and mixed with 1 ml 25% aqueous ammonia for ca 30 min. The reaction mixture was partitioned between water and ethyl acetate. The phases were separated and the organic phase was purified by chromatography on silica gel with ethyl acetate:heptane=1:3 to yield 0.16 g of the title compound as oil. MS (ISN) M−H+=232.0

後処理

  1. temperatureThe mixture was cooled to room temperature
  2. temperatureThe mixture was heated to 55° C. for ca 30 min
  3. temperaturecooled to room temperature and poored onto ice
  4. extractionextracted with ethyl acetate
  5. customthe phases were separated
  6. washthe organic phase was washed with water and brine
  7. customevaporated
  8. additionmixed with 1 ml 25% aqueous ammonia for ca 30 min
  9. customThe reaction mixture was partitioned between water and ethyl acetate
  10. customThe phases were separated
  11. customthe organic phase was purified by chromatography on silica gel with ethyl acetate

出典と根拠

ORDレコード
ord-86fe7fe0b98c49f6b21c34fa85a6dbcc
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08163778B2

反応ノート

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