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Stannous Chloride → 5-bromo-N1-(3-methoxypropyl)benzene-1,2-diamine

HRID 2263530
ノート
印刷プレビュー

反応式

HRID 2263530 の反応式
[Sn](Cl)Cl.[Br:4][C:5]1[CH:6]=[CH:7][C:8]([N+:17]([O-])=O)=[C:9]([NH:11][CH2:12][CH2:13][CH2:14][O:15][CH3:16])[CH:10]=1>C(O)C>[Br:4][C:5]1[CH:10]=[C:9]([NH:11][CH2:12][CH2:13][CH2:14][O:15][CH3:16])[C:8]([NH2:17])=[CH:7][CH:6]=1
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 24479Stannous ChlorideHCID 65341496(5-Bromo-2-nitrophenyl)(3-methoxypropyl)amine

生成物 1

HCID 653434125-bromo-N1-(3-methoxypropyl)benzene-1,2-diamine

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

78.57 g of tin(II) chloride are added to a solution of 21.01 g of (5-bromo-2-nitrophenyl)-(3-methoxypropyl)amine in 950 ml of ethanol. The reaction mixture is heated to reflux for 12 hours. The mixture is cooled to room temperature and concentrated by evaporation. The residue is treated with 2M NaOH until a pH of 11 has been attained. The mixture is extracted with tert-butyl methyl ether (3×). The combined organic phases are dried with sodium sulphate and concentrated by evaporation. The title compound is obtained as an orange oil from the residue. Rf=0.31 (1:1 EtOAc-heptane). Rt=3.06 (gradient I).

後処理

  1. temperatureThe reaction mixture is heated
  2. temperatureto reflux for 12 hours
  3. concentrationconcentrated by evaporation
  4. additionThe residue is treated with 2M NaOH until a pH of 11
  5. extractionThe mixture is extracted with tert-butyl methyl ether (3×)
  6. dry with materialThe combined organic phases are dried with sodium sulphate
  7. concentrationconcentrated by evaporation

出典と根拠

ORDレコード
ord-f2fd000caa8a44e0aaf3078c14ce78b0
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07851634B2

反応ノート

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