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Dimethylformamide → HCID 82677013、化合物

HRID 2405653
ノート
印刷プレビュー

反応式

HRID 2405653 の反応式
C([N:4]([CH2:8][CH3:9])[CH:5]([CH3:7])C)(C)C.IC[C:12]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19]C)=[CH:14][CH:13]=1.S([O-])([O-])(=O)=[O:22].[Mg+2].CN([CH:30]=[O:31])C>>[CH2:14]([C:15]1[CH:18]=[CH:19][C:9]([CH2:8][NH:4][CH2:5][C:7]([O:31][CH3:30])=[O:22])=[CH:17][CH:16]=1)[CH2:13][CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 6228DimethylformamideHCID 24083Sulfuric acid magnesium salt (1:1)HCID 81531DiisopropylethylamineHCID 86690145HCID 86690145、化合物

生成物 1

HCID 82677013HCID 82677013、化合物収率 77%

実験手順

Under argon condition, glycine methyl ether (448 mg, 3.57 mmol) was dissolved in 5 mL of dry DMF and then N,N-diisopropylethylamine (DIPEA; 777 μL, 4.46 mmol) and 1-(iodomethyl)-4-propylbenzene (232 mg, 0.892 mmol) were added. The reaction mixture was then stirred for one day at room temperature. Upon completion of the reaction, the reaction was terminated by adding 10 mL of water and the reaction mixture was extracted with diethyl ether (10 mL×4). The organic layer thus obtained was treated with anhydrous magnesium sulfate to remove water. The precipitate was filtered out and the resulting solution was concentrated by distillation under reduced pressure and purified by column chromatography to obtain 152 mg (0.687 mmol, 77%) of the desired compound.

後処理

  1. customUpon completion of the reaction
  2. customthe reaction was terminated
  3. additionby adding 10 mL of water
  4. extractionthe reaction mixture was extracted with diethyl ether (10 mL×4)
  5. customThe organic layer thus obtained
  6. customto remove water
  7. filtrationThe precipitate was filtered out
  8. concentrationthe resulting solution was concentrated by distillation under reduced pressure
  9. custompurified by column chromatography

出典と根拠

ORDレコード
ord-2cc6d6f0652d4787948acaa31b6ce525
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08809012B2

反応ノート

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