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Potassium thiocyanate → (2,2-Dichloro-3,3-dimethylcyclopropyl)methyl thiocyanate

HRID 1981332
ノート
印刷プレビュー

反応式

HRID 1981332 の反応式
[Cl:1][C:2]1([Cl:9])[C:4]([CH3:6])([CH3:5])[CH:3]1[CH2:7]Cl.[S-:10][C:11]#[N:12].[K+]>C(O)C>[Cl:1][C:2]1([Cl:9])[C:4]([CH3:6])([CH3:5])[CH:3]1[CH2:7][S:10][C:11]#[N:12]
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 516872Potassium thiocyanateHCID 27752731,1-Dichloro-3-(chloromethyl)-2,2-dimethylcyclopropane

生成物 1

HCID 13313519(2,2-Dichloro-3,3-dimethylcyclopropyl)methyl thiocyanate収率 85.9%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

1.87 g of 2,2-dichloro-3,3-dimethyl-1-chloromethylcyclopropane and 1.0 g of potassium thiocyanate were suspended in 20 ml of ethanol, and the suspension was refluxed for 12 hours. Ethanol was evaporated, and 20 ml of water was added. The mixture was extracted with toluene. The toluene layer was washed with water and dried over sodium sulfate. The toluene was then evaporated under reduced pressure to give 1.80 g of 2,2-dichloro-3,3-dimethylcyclopropylmethyl thiocyanate, the desired compound shown above. The boiling point of the product was 115° C. at 200 mmHg.

後処理

  1. temperaturethe suspension was refluxed for 12 hours
  2. customEthanol was evaporated
  3. addition20 ml of water was added
  4. extractionThe mixture was extracted with toluene
  5. washThe toluene layer was washed with water
  6. dry with materialdried over sodium sulfate
  7. customThe toluene was then evaporated under reduced pressure

出典と根拠

ORDレコード
ord-b3a5eab249d44e83841cdbc99e247a0d
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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