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Sulfuric Acid → 2,2'-Azobis(2,4-dimethylvaleronitrile)

HRID 1680124
ノート
印刷プレビュー

反応式

HRID 1680124 の反応式
[NH2:1][C:2]([CH3:9])([CH2:5][CH:6]([CH3:8])[CH3:7])[C:3]#[N:4].Cl[O-].[Na+].S(=O)(=O)(O)O.S(=O)(O)[O-].[Na+]>O.C(OCC)(=O)C>[N:1]([C:2]([CH3:9])([CH2:5][CH:6]([CH3:8])[CH3:7])[C:3]#[N:4])=[N:1][C:2]([CH3:9])([CH2:5][CH:6]([CH3:8])[CH3:7])[C:3]#[N:4]
参加物反応条件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 1118Sulfuric AcidHCID 922512-Amino-2,4-dimethylpentanenitrileHCID 23665760Sodium HypochloriteHCID 23665763Sodium Bisulfite

生成物 1

HCID 915372,2'-Azobis(2,4-dimethylvaleronitrile)

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回
HCID 8857
Ethyl Acetate
溶媒

反応条件

温度
15 °C

実験手順

In the same manner as in Example 1, 2-amino-2,4-dimethylpentanonitrile and sodium hypochlorite were reacted. By iodometry, it was found that the total oxidative compounds in both the water and ethyl acetate phases after reaction was 0.05 equivalent. The reaction mixture was adjusted to a pH of 6 with a dilute sulfuric acid, and a solution of 6.5 g (0.125 equivalent) of sodium bisulfite in 30 ml of water was added thereto. The resulting mixture was stirred at 15° C. for 30 minutes to effect the reduction. Thereafter, the ethyl acetate phase was separated from the water phase, and the ethyl acetate in the organic phase was removed by distillation. Water was added to the residue and precipitated white crystals were filtered, washed with water and dried to obtain 26.0 g of 2,2'-azobis(2,4-dimethylvaleronitrile). Yield was 89 mole %. The product was analyzed by iodometry, and it was found that the amount of oxidative impurities was 100 ppm or less and that the purity of the product was 99.5%.

後処理

  1. customafter reaction
  2. customThereafter, the ethyl acetate phase was separated from the water phase
  3. customthe ethyl acetate in the organic phase was removed by distillation
  4. additionWater was added to the residue
  5. customprecipitated white crystals
  6. filtrationwere filtered
  7. washwashed with water
  8. customdried

出典と根拠

ORDレコード
ord-84c7bdfa22364d32b0649b190f9ec153
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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