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Acetone → Diisopropylether hexane

HRID 2052551
ノート
印刷プレビュー

反応式

HRID 2052551 の反応式
C[C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[N+]#[C-].C(#N)C.ClCl.[N-]=[N+]=[N-].[Na+].[CH3:20][C:21]([CH3:23])=[O:22]>O>[CH:21]([O:22][CH:6]([CH3:7])[CH3:8])([CH3:23])[CH3:20].[CH3:6][CH2:7][CH2:2][CH2:3][CH2:4][CH3:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 180AcetoneHCID 6342AcetonitrileHCID 24526ChlorineHCID 33557Sodium AzideHCID 42121842,4-Dimethylphenylisocyanide

生成物 1

HCID 21881879Diisopropylether hexane

試薬・触媒・溶媒 1

HCID 962Water
溶媒

実験手順

A solution of 2,4-dimethylphenylisonitrile (Ugi, et al., Angew. Chem. Internat. Ed. (Engl.) 4, 472 (1965)) (14.8 g., 0.11 mole) in 100 ml. of acetonitrile was stirred at ice bath temperature while chlorine gas was bubbled in. When tlc indicated that the isonitrile had been consumed, the solvent was removed in vacuo, leaving 22.7 g. of the oily isocyanodichloride. To a solution of the latter in 130 ml. of acetone was added a solution of 7.3 g. (0.11 mole) of sodium azide in 25 ml. of water. After one hour, the acetone was evaporated in vacuo and the aqueous residue was extracted with ethyl acetate. The extract was washed with water and brine, dried (Na2SO4) and evaporated to provide 24.5 g. of a waxy solid. Trituration with isopropyl ether-hexane gave 18.9 g. of the chlorotetrazole, m.p. 75°-77°.

後処理

  1. customwas bubbled in
  2. customhad been consumed
  3. customthe solvent was removed in vacuo
  4. customleaving 22.7 g
  5. customthe acetone was evaporated in vacuo
  6. extractionthe aqueous residue was extracted with ethyl acetate
  7. washThe extract was washed with water and brine
  8. dry with materialdried (Na2SO4)
  9. customevaporated
  10. customto provide 24.5 g

出典と根拠

ORDレコード
ord-1aafa836dd564e23bb2a17d445c46b98
出典データセット
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04186131

反応ノート

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