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Ethyl bromoacetate → ethyl 3,5-diethyl-1H-pyrazole-1-acetate

HRID 2043750
ノート
印刷プレビュー

反応式

HRID 2043750 の反応式
[CH2:1]([C:3]1[CH2:7][C:6]([CH2:8][CH3:9])=[N:5][N:4]=1)[CH3:2].C(C1C=C(CC)NN=1)C.C(=O)([O-])[O-].[K+].[K+].Br[CH2:26][C:27]([O:29][CH2:30][CH3:31])=[O:28]>CN(C)C=O>[CH2:1]([C:3]1[CH:7]=[C:6]([CH2:8][CH3:9])[N:5]([CH2:26][C:27]([O:29][CH2:30][CH3:31])=[O:28])[N:4]=1)[CH3:2]
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 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 43063673,5-diethyl-1H-pyrazoleHCID 588905493,5-diethyl-4H-pyrazole

生成物 1

HCID 67458757ethyl 3,5-diethyl-1H-pyrazole-1-acetate収率 77.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

To a solution of 3,5-diethyl-4H-pyrazole (2.14 g, 17.2 mmol) (i.e. the product of Example 15, Step A) in N,N-dimethylformamide (10 mL) was added potassium carbonate (4.7 g) and ethyl bromoacetate (2.9 mL, 26.1 mmol). The reaction mixture was stirred at room temperature overnight. The resulting solids were filtered off and the filtrate was diluted with ethyl acetate, washed with water and dried over MgSO4. The reaction mixture was concentrated under reduced pressure to give 2.79 g of the title compound.

後処理

  1. filtrationThe resulting solids were filtered off
  2. additionthe filtrate was diluted with ethyl acetate
  3. washwashed with water
  4. dry with materialdried over MgSO4
  5. concentrationThe reaction mixture was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-c5299b6f51fa4d7dbec6aa7a94348034
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08586611B2

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