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2-Nitropropane → HCID 59355188、化合物

HRID 1023492
ノート
印刷プレビュー

反応式

HRID 1023492 の反応式
[N+:1]([CH:4]([CH3:6])[CH3:5])([O-:3])=[O:2].[CH3:7][N:8]([CH3:12])[CH2:9][CH2:10][NH2:11].[OH-].[Na+].[CH2:15]=O>CC(O)C.O>[CH3:7][N:8]([CH3:12])[CH2:9][CH2:10][NH:11][CH2:5][C:4]([CH3:15])([N+:1]([O-:3])=[O:2])[CH3:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 3982-NitropropaneHCID 712FormaldehydeHCID 14798Sodium HydroxideHCID 66053N,N-Dimethylethylenediamine

生成物 1

HCID 59355188HCID 59355188、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒3 回
HCID 3776
Isopropanol
溶媒

実験手順

To a solution of 2-nitropropane (2.07 g, 23.2 mmol) and N1,N1-dimethyl-ethane-1,2-diamine (2.22 g, 25.2 mmol) in 2-propanol (5 ml) was added 5 M NaOH in H2O (30 ul, 0.15 mmol), H2O (1 ml). 37% Formaldehyde in H2O (1.8 ml, 24 mmol) was added dropwise, and the reaction stirred for 22 h. The solution was concentrated in vacuo to half volume, acidified with sat. NaHSO4 to pH 2, and washed with 3× 100 ml CH2Cl2. 15% NaOH in H2O was added to pH 12, and the slurry extracted with 3× 100 ml CH2Cl2. The organic phases were combined, dried on MgSO4, concentrated in vacuo, and used without further purification. ESI/APCI (pos) expected for C8H19N3O2: 189.15. Found: 190 (MH+).

後処理

  1. concentrationThe solution was concentrated in vacuo to half volume
  2. washwashed with 3× 100 ml CH2Cl2
  3. addition15% NaOH in H2O was added to pH 12
  4. extractionthe slurry extracted with 3× 100 ml CH2Cl2
  5. customdried on MgSO4
  6. concentrationconcentrated in vacuo
  7. customused without further purification

出典と根拠

ORDレコード
ord-88be1e0339e94bcaa0ac2aa683822073
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08722715B2

反応ノート

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