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Water → 3-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]butanoic acid

HRID 639828
ノート
印刷プレビュー

反応式

HRID 639828 の反応式
O.OS(O)(=O)=O.[Cl:7][C:8]1[CH:9]=[C:10]([C:14]2[N:15]=[N:16][N:17]([CH:19]([CH3:23])[CH2:20][CH2:21][OH:22])[N:18]=2)[CH:11]=[CH:12][CH:13]=1.CC([OH:27])C>CC(C)=O>[Cl:7][C:8]1[CH:9]=[C:10]([C:14]2[N:15]=[N:16][N:17]([CH:19]([CH3:23])[CH2:20][C:21]([OH:27])=[O:22])[N:18]=2)[CH:11]=[CH:12][CH:13]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 1118Sulfuric AcidHCID 3776IsopropanolHCID 684296013-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]butan-1-ol

生成物 1

HCID 684316183-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]butanoic acid収率 100%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A mixture of CrO3 (0.46 g, 4.63 mmol), H2O (2.5 mL) and concentrated H2SO4 (0.46 mL) was added to a solution of 3-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]butan-1-ol (0.9 g, 3.6 mmol) in acetone (30 mL) at 0° C. The reaction was stirred at r.t. for 1.5 h. 2-Propanol was added and the mixture was concentrated. Sat. NaCl (25 mL) and EtOAc (50 mL) were added to the residue and the mixture was extracted. The water phase was re-extracted with EtOAc (50 mL) and the combined organic phases were dried (MgSO4) and concentrated to give 0.95 g (100%) of the title compound.

後処理

  1. concentrationthe mixture was concentrated
  2. additionSat. NaCl (25 mL) and EtOAc (50 mL) were added to the residue
  3. extractionthe mixture was extracted
  4. extractionThe water phase was re-extracted with EtOAc (50 mL)
  5. dry with materialthe combined organic phases were dried (MgSO4)
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-ea7226872a9e4c4b802a45a8835aaf68
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07691892B2

反応ノート

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