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Chlorine → HCID 178478025、化合物

HRID 1376319
ノート
印刷プレビュー

反応式

HRID 1376319 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:12]=[CH:11][NH:10][N:9]=1.[Cl:13]Cl>C(O)(=O)C.C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[C:12]([Cl:13])=[CH:11][NH:10][N:9]=1
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 2

HCID 24526ChlorineHCID 178478013HCID 178478013、化合物

生成物 1

HCID 178478025HCID 178478025、化合物収率 44.5%

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒2 回HCID 6344Dichloromethane溶媒

実験手順

6.8 g (0.038 mol) of 3-(2'-chlorophenyl)-1H-pyrazole, prepared as in Example 9, are dissolved, at temperature and with stirring, in 30 ml of acetic acid. 2.9 g (0.0409 mol) of chlorine are then introduced into the reaction mixture. Stirring is maintained for 1 hour at room temperature and then the acetic acid is driven off under reduced pressure. The residue is taken up in methylene chloride and this organic solution is washed with in aqueous bicarbonate solution, then with water and then dried over Na2SO4 before being concentrated to dryness. The residue is chromatographed on a silica column (eluent: heptane/ethyl acetate 60/40). 3.6 g of 3-(2'-chlorophenyl)-4-chloro-1H-pyrazole (compound 96) are obtained, which is of honey-like consistency (yield 44%).

後処理

  1. dissolutionare dissolved, at temperature
  2. washthis organic solution is washed with in aqueous bicarbonate solution
  3. dry with materialwith water and then dried over Na2SO4
  4. concentrationbefore being concentrated to dryness
  5. customThe residue is chromatographed on a silica column (eluent: heptane/ethyl acetate 60/40)

出典と根拠

ORDレコード
ord-44e8366371f34efb9606df81416b8b9a
出典データセット
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05663119

反応ノート

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