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Triethylamine → 2-Diazocyclohexane-1,3-dione

HRID 1727248
ノート
印刷プレビュー

反応式

HRID 1727248 の反応式
C(NC1C=CC(S([N:14]=[N+:15]=[N-])(=O)=O)=CC=1)(=O)C.C(N(CC)CC)C.[C:24]1(=[O:31])[CH2:29][CH2:28][CH2:27][C:26](=[O:30])[CH2:25]1>ClCCl>[N+:14](=[C:25]1[C:26](=[O:30])[CH2:27][CH2:28][CH2:29][C:24]1=[O:31])=[N-:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 104341,3-CyclohexanedioneHCID 51291854-Acetamidobenzenesulfonyl azide

生成物 1

HCID 110624492-Diazocyclohexane-1,3-dione

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A mixture of 4-acetamidobenzenesulphonylazide (25 g, 104 mmol) and triethylamine (36 ml, 250 mmol) in dichloromethane maintained at a temperature below 30° C. by external cooling is treated dropwise by a solution of cyclohexane-1,3-dione (13 g, 115 mmol) in 200 ml of dichloromethane. The reaction mixture is stirred for 75 minutes at ambient temperature then filtered on Celite. After concentration to approximately 300 ml, the filtrate is washed with water then dried over sodium sulphate. The brown-yellow solid (14 g; 88%) obtained by evaporation of the solvent under reduced pressure is similar to that obtained in Example 55.1, and is used as it is in the following stage.

後処理

  1. temperaturemaintained at a temperature below 30° C.
  2. temperatureby external cooling
  3. filtrationthen filtered on Celite
  4. concentrationAfter concentration to approximately 300 ml
  5. washthe filtrate is washed with water
  6. dry with materialthen dried over sodium sulphate
  7. customThe brown-yellow solid (14 g; 88%) obtained by evaporation of the solvent under reduced pressure
  8. customthat obtained in Example 55.1

出典と根拠

ORDレコード
ord-48956b759ef4424a801790be8f20d1fb
出典データセット
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07495021B2

反応ノート

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