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Ammonium Chloride → methyl 2-(2H-tetrazol-5-yl)benzoate

HRID 1658459
ノート
印刷プレビュー

反応式

HRID 1658459 の反応式
[C:1]([C:3]1[CH:12]=[CH:11][CH:10]=[CH:9][C:4]=1[C:5]([O:7][CH3:8])=[O:6])#[N:2].[N-:13]=[N+:14]=[N-:15].[Na+].[Cl-].[NH4+]>>[N:2]1[NH:13][N:14]=[N:15][C:1]=1[C:3]1[CH:12]=[CH:11][CH:10]=[CH:9][C:4]=1[C:5]([O:7][CH3:8])=[O:6]
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 3

HCID 25517Ammonium ChlorideHCID 33557Sodium AzideHCID 582554Methyl 2-cyanobenzoate

生成物 1

HCID 21527413methyl 2-(2H-tetrazol-5-yl)benzoate

実験手順

Methyl 2-cyanobenzoate (54 g, 0.33 mole) in D.M.F. (165 ml) was treated with sodium azide (23.4 g, 0.36 mole) and ammonium chloride (19.3 g, 0.36 mole). After the reaction mixture had been stirred on the steam bath for 20 hrs., the D.M.F. was removed under reduced pressure and the residue dissolved in water (200 ml). The solution was filtered, cooled in ice and acidified to give a white precipitate which was filtered, washed with water and dried. This gave methyl 2-(5-2H-tetrazolyl)benzoate, M.P. 132°-5°, 19 g (28%). (Found: C, 53.79, 52.59, 52.33; H, 4.25, 4.17, 4.07; N, 26.79, 26.84, 27.25. C9H8N4O2 requires C, 52.94; H, 3.95; N, 27.44.)

後処理

  1. customwas removed under reduced pressure
  2. dissolutionthe residue dissolved in water (200 ml)
  3. filtrationThe solution was filtered
  4. temperaturecooled in ice
  5. customto give a white precipitate which
  6. filtrationwas filtered
  7. washwashed with water
  8. customdried

出典と根拠

ORDレコード
ord-0944ccf091a141868a777fe897507993
出典データセット
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03964896

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート