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Water → methyl 5-(4-bromo-2-formyl-N-propylanilino)pentanoate

HRID 1928928
ノート
印刷プレビュー

反応式

HRID 1928928 の反応式
[Br:1][C:2]1[CH:18]=[CH:17][C:5]([N:6]([CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])[CH2:7][CH2:8][CH3:9])=[C:4]([CH:19]=[O:20])[CH:3]=1.[C:21](=O)([O-])[O-].[K+].[K+].IC.O>CN(C=O)C>[Br:1][C:2]1[CH:18]=[CH:17][C:5]([N:6]([CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16][CH3:21])=[O:15])[CH2:7][CH2:8][CH3:9])=[C:4]([CH:19]=[O:20])[CH:3]=1
参加物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 962WaterHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 865955795-(4-bromo-2-formyl-N-propylanilino)pentanoic acid

生成物 1

HCID 86595580methyl 5-(4-bromo-2-formyl-N-propylanilino)pentanoate収率 94.7%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒
2 回

実験手順

To a suspension of 5-(4-bromo-2-formyl-N-propylanilino)pentanoic acid (8.00 g) and potassium carbonate (3.88 g) in DMF (25 ml) was added dropwise a solution of iodomethane (4.66 g) in DMF (5 ml) under a nitrogen atmosphere. The mixture was stirred overnight under a nitrogen atmosphere. Then, water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over magnesium sulfate. The solvent was distilled off under reduced pressure to obtain brown oil of methyl 5-(4-bromo-2-formyl-N-propylanilino)pentanoate (7.89 g).

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with saturated saline
  3. dry with materialdried over magnesium sulfate
  4. distillationThe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-e4a6752e0ce449299ebc2b4055f2887f
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08183273B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート