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HCID 17954114、化合物 → 460078-00-6

HRID 1774140
ノート
印刷プレビュー

反応式

HRID 1774140 の反応式
[N:1]([CH2:4][CH2:5][CH:6]([CH2:12][CH2:13][N:14]=[N+]=[N-])[CH2:7][CH2:8][N:9]=[N+]=[N-])=[N+]=[N-].[H][H]>C(O)C.[Pd]>[NH2:1][CH2:4][CH2:5][CH:6]([CH2:12][CH2:13][NH2:14])[CH2:7][CH2:8][NH2:9]
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 2

HCID 17954114HCID 17954114、化合物HCID 178418361HCID 178418361、化合物

生成物 1

HCID 9942175460078-00-6収率 100%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

Tris(2-azidoethyl)methane (15.06 g, 0.0676 mol), (assuming 100% yield from previous reaction) in ethanol (200 ml) was treated with 10% palladium on charcoal (2 g, 50% water) and hydrogenated for 12 h. The reaction vessel was evacuated every 2 hours to remove nitrogen evolved from the reaction and refilled with hydrogen. A sample was taken for NMR analysis to confirm complete conversion of the triazide to the triamine. Caution: unreduced azide could explode on distillation. The reaction was filtered through a celite pad to remove the catalyst and concentrated in vacuo to give tris(2-aminoethyl)methane as an oil. This was further purified by Kugelrohr distillation bp. 180-200° C. at 0.4 mm/Hg to give a colourless oil (8.1 g, 82.7% overall yield from the triol).

後処理

  1. customThe reaction vessel was evacuated every 2 hours
  2. customto remove nitrogen
  3. customevolved from the reaction
  4. distillationCaution: unreduced azide could explode on distillation
  5. filtrationThe reaction was filtered through a celite pad
  6. customto remove the catalyst
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-322c15d823ce49f4b04b7ccc8dcd9472
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09259496B2

反応ノート

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