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Ammonia → 2-Amino-2,4-dimethylpentanenitrile

HRID 1680122
ノート
印刷プレビュー

反応式

HRID 1680122 の反応式
[NH3:1].O[C:3]([CH3:10])([CH2:6][CH:7]([CH3:9])[CH3:8])[C:4]#[N:5]>O>[NH2:1][C:3]([CH3:10])([CH2:6][CH:7]([CH3:9])[CH3:8])[C:4]#[N:5]
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 222AmmoniaHCID 1072302-Hydroxy-2,4-dimethylpentanenitrile

生成物 1

HCID 922512-Amino-2,4-dimethylpentanenitrile

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a 1-liter autoclave were added 7 moles of ammonia and then 3.5 moles of 90%-pure 2-hydroxy-2,4-dimethylpentanonitrile, and the mixture was reacted at 27° C. for 10 hours at a rate of 300 r.p.m. Thus, 2-amino-2,4-dimethylpentanonitrile was synthesized. After reaction, the reaction mixture was taken out of the autoclave, and 44 g of the water phase was separated. The residue was distilled in a wetted wall tower under the following conditions: Temperature of the heating portion 25° C.; pressure 30 mmHg; and residence time in the heating portion 1 minute or less. Low-boiling compounds were thus distilled off and purified 2-amino-2,4-dimethylpentanonitrile was withdrawn from the bottom. The yield of the purified product was 90.0 mole % based on cyanohydrin. This purified product contained 0.5% by weight of ammonia and 0.8% by weight of hydrogen cyanide, and its purity was 90%.

後処理

  1. customAfter reaction
  2. customwas separated
  3. distillationThe residue was distilled in a wetted wall tower under the following conditions
  4. customTemperature of the heating portion 25° C.
  5. customin the heating portion 1 minute or less
  6. distillationwere thus distilled off
  7. custompurified 2-amino-2,4-dimethylpentanonitrile
  8. customwas withdrawn from the bottom

出典と根拠

ORDレコード
ord-b8876ba487894cda80e0fd7f7c84600d
出典データセット
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04272435

反応ノート

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