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Water → (2,2-Dichloro-3,3-dimethylcyclopropyl)acetonitrile

HRID 1981334
ノート
印刷プレビュー

反応式

HRID 1981334 の反応式
C1(C)C=CC(S(O[CH2:11][CH:12]2[C:14]([CH3:16])([CH3:15])[C:13]2([Cl:18])[Cl:17])(=O)=O)=CC=1.[C-:20]#[N:21].[K+].O>CN(C)C=O>[Cl:18][C:13]1([Cl:17])[C:14]([CH3:15])([CH3:16])[CH:12]1[CH2:11][C:20]#[N:21]
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

5

反応物 3

HCID 962WaterHCID 9032Potassium CyanideHCID 13313521HCID 13313521、化合物

生成物 1

HCID 13313532(2,2-Dichloro-3,3-dimethylcyclopropyl)acetonitrile収率 106.5%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

6.48 g of 2,2-dichloro-3,3-dimethylcyclopropylmethyl p-toluenesulfonate and 2.0 g of potassium cyanide were suspended in 20 ml of dimethyl formamide, and the mixture was heated at 100° C. for 24 hours with stirring. After cooling, 50 ml of water was added to the reaction mixture. The mixture was extracted with hexane. The hexane layer was washed with water, and dried over sodium sulfate. After drying, the hexane was evaporated under reduced pressure to give 3.8 g of 2,2-dichloro-3,3-dimethylcyclopropylacetonitrile, the desired compound shown above. The boiling point of the product was 96° to 98° C. at 14 mmHg.

後処理

  1. temperatureAfter cooling
  2. extractionThe mixture was extracted with hexane
  3. washThe hexane layer was washed with water
  4. dry with materialdried over sodium sulfate
  5. customAfter drying
  6. customthe hexane was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-be4af018903341bd8ac5651fc55f3388
出典データセット
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04514418

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート