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diethyl 1H-pyrazole-3,5-dicarboxylate → diethyl 4-chloro-1H-pyrazole-3,5-dicarboxylate

HRID 2046230
ノート
印刷プレビュー

反応式

HRID 2046230 の反応式
[Cl:1][O-].[Na+].[NH:4]1[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:7][C:6]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[N:5]1>CC(O)=O>[CH2:12]([O:11][C:9]([C:8]1[C:7]([Cl:1])=[C:6]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[NH:5][N:4]=1)=[O:10])[CH3:13]
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 2

HCID 142184diethyl 1H-pyrazole-3,5-dicarboxylateHCID 23665760Sodium Hypochlorite

生成物 1

HCID 67975929diethyl 4-chloro-1H-pyrazole-3,5-dicarboxylate収率 77.3%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

Sodium hypochlorite (2.79 mL, 5.89 mmol) was added to a solution of diethyl 3,5-pyrazoledicarboxylate (0.5 g, 2.36 mmol) in AcOH (10 mL) and the mixture was stirred at room temperature for 16 hours. Then, the solvent was evaporated in vacuo and the mixture was acidified with a 1N solution of HCl and extracted with AcOEt. The organic layer was separated, dried (MgSO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 05/95). The desired fractions were collected and the solvents evaporated in vacuo to yield 4-chloro-1H-pyrazole-3,5-dicarboxylic acid diethyl ester (450 mg, 66% yield) as a white solid.

後処理

  1. customThen, the solvent was evaporated in vacuo
  2. extractionextracted with AcOEt
  3. customThe organic layer was separated
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customthe solvents evaporated in vacuo
  7. customThe crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 05/95)
  8. customThe desired fractions were collected
  9. customthe solvents evaporated in vacuo

出典と根拠

ORDレコード
ord-02ea0c77547f417f802fc233d7a234f6
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08592422B2

反応ノート

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