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Dimethylamine → N,N-dimethyl-5-methoxy-2-bromophenylacetamide

HRID 1270787
ノート
印刷プレビュー

反応式

HRID 1270787 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([Br:13])=[C:7]([CH2:9][C:10](Cl)=[O:11])[CH:8]=1.[CH3:14][NH:15][CH3:16]>CCOCC>[CH3:14][N:15]([CH3:16])[C:10](=[O:11])[CH2:9][C:7]1[CH:8]=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][C:6]=1[Br:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 674DimethylamineHCID 184515295-Methoxy-2-bromophenylacetyl chloride

生成物 1

HCID 18451566N,N-dimethyl-5-methoxy-2-bromophenylacetamide

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

5-Methoxy-2-bromophenylacetyl chloride (60 g, 0.23 mol) is dissolved in anhydrous Et2O (400 mL), stirred and cooled in an ice bath. A 2 M solution of dimethylamine (228 mL, 0.46 mol) is added dropwise and the mixture allowed to warm to room temperature and stirred for 2 hours. Additional Et2O (500 mL) is added. The organic solution is washed with 1 N HCl (2×500 mL), saturated NaHCO3 (500 mL) and brine (500 mL). The organic layer is dried (Na2SO4) and concentrated by rotary evaporator. The residue is purified using flash chromatography (hexanes/EtOAc, from 7:3 to 1:9). Trituration of the crude product with Et2O/hexanes gives N,N-dimethyl-5-methoxy-2-bromophenylacetamide as a white crystalline solid (m.p. 88–90° C.).

後処理

  1. temperaturecooled in an ice bath
  2. stirringstirred for 2 hours
  3. washThe organic solution is washed with 1 N HCl (2×500 mL), saturated NaHCO3 (500 mL) and brine (500 mL)
  4. dry with materialThe organic layer is dried (Na2SO4)
  5. concentrationconcentrated by rotary evaporator
  6. customThe residue is purified

出典と根拠

ORDレコード
ord-004c3462ebdf41948f00335f39e12ac2
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07202364B2

反応ノート

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