Hydrazoic acid → HCID 178420316、化合物

HRID 2057894

反応式

HRID 2057894 の反応式
[CH2:1]([N:8]1[CH:12]=[CH:11][N:10]=[C:9]1[CH:13]=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl-].[NH4+].[N-]=[N+]=[N-].[Na+].C(N1C=CN=C1C#N)C1C=CC=CC=1.N=[N+]=[N-].[NH:38]1C=[N:41][N:40]=[N:39]1>CN(C)C=O.O>[CH2:1]([N:8]1[CH:12]=[CH:11][N:10]=[C:9]1[C:13]1[NH:41][N:40]=[N:39][N:38]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

9

実験手順

Obtained by reacting 9.3 g (0.05 mol) of 1-benzyl-2-formylimidazole (see Liebigs Ann. Chem. 718 (1968) pp. 249-259) with 8.0 g (0.15 mol) of ammonium chloride and 9.8 g (0.15 mol) of sodium azide in 50 ml of dimethylformamide at 120°-130° C. The isolation of the 1-benzyl-2-cyanoimidazole intermediate (obtained by Schmidt-rearrangement) may be omitted, since this compound adds excess hydrazoic acid to the tetrazole in situ. After 20 hours, it is cooled, and 500 ml of water are added, the precipitate formed filtered off and recrystallised several times from dimethylformamide. M.p. 274°-275° C.

後処理

  1. customObtained
  2. customat 120°-130° C
  3. temperatureit is cooled
  4. customthe precipitate formed
  5. filtrationfiltered off
  6. customrecrystallised several times from dimethylformamide

出典と根拠

ORDレコード
ord-1a0a0e1e24884fef88d6adf35ec1d162
出典データセット
uspto-grants-1980_07
特許番号
US04213986

関連ノート

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