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Hydrochloric Acid → 4-Chloro-6-cyclopropyl-1,3,5-triazin-2-amine

HRID 329454
ノート
印刷プレビュー

反応式

HRID 329454 の反応式
[Na].[C:2]([NH:4][C:5]([CH:9]1[CH2:11][CH2:10]1)=[N:6][C:7]#[N:8])#[N:3].[ClH:12].CCCCCC>CC(=O)CC>[NH2:8][C:7]1[N:3]=[C:2]([Cl:12])[N:4]=[C:5]([CH:9]2[CH2:11][CH2:10]2)[N:6]=1
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

6

反応物 4

HCID 313Hydrochloric AcidHCID 8058HexaneHCID 5360545SodiumHCID 19872211N,N'-Dicyano-cyclopropanecarbamidine

生成物 1

HCID 198722124-Chloro-6-cyclopropyl-1,3,5-triazin-2-amine

試薬・触媒・溶媒 1

HCID 6569Methyl Ethyl Ketone溶媒2 回

反応条件

温度
10 °C

実験手順

33 g of the sodium salt of N,N'-dicyano-cyclopropanecarbamidine (crude product) is suspended in 100 ml butanone. A solution of 20 g HCl in 400 ml butanone is dropped under stirring into this solution at 10° C. After the addition has been completed it is stirred for 1 h at ambient temperature. The reaction mixture is concentrated by evaporation and 200 ml of saturated aqueous NaHCO3 -solution and 300 ml diethylether are added. The organic phase is separated, washed, dried and concentrated by evaporation. One isolates 21 g of crude product which is treated with hexane to leave the pure title product.

後処理

  1. additionAfter the addition
  2. stirringis stirred for 1 h at ambient temperature
  3. concentrationThe reaction mixture is concentrated by evaporation and 200 ml of saturated aqueous NaHCO3 -solution and 300 ml diethylether
  4. additionare added
  5. customThe organic phase is separated
  6. washwashed
  7. customdried
  8. concentrationconcentrated by evaporation
  9. customOne isolates 21 g of crude product which

出典と根拠

ORDレコード
ord-9c52b814efe34122964a2622207880d0
出典データセット
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04891443

反応ノート

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