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Tetrahydrofuran → Ethyl 4-(2,4-dichlorophenyl)-2,4-dioxobutanoate

HRID 1166174
ノート
印刷プレビュー

反応式

HRID 1166174 の反応式
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([Cl:10])=[CH:6][C:5]=1[Cl:11])=[O:3].C([N-]C(C)C)(C)C.[Li+].[C:20]([O:23][CH2:24][C:25](Cl)=[O:26])(=O)[CH3:21].C1C[O:31]CC1>>[Cl:11][C:5]1[CH:6]=[C:7]([Cl:10])[CH:8]=[CH:9][C:4]=1[C:2](=[O:3])[CH2:1][C:25](=[O:26])[C:24]([O:23][CH2:20][CH3:21])=[O:31]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 8028TetrahydrofuranHCID 166932',4'-DichloroacetophenoneHCID 26297Acetoxyacetyl chlorideHCID 2724682Lithium diisopropylamide

生成物 1

HCID 22997478Ethyl 4-(2,4-dichlorophenyl)-2,4-dioxobutanoate

反応条件

温度
-78 °C

実験手順

A solution of 2,4-dichloroacetophenone (3.78 g) in THF (20 ml) was cooled to −78° C. under a nitrogen atmosphere. To this stirred solution was added lithium diisopropylamide (LDA) (1.0 M, 22 ml) and the resulting solution was stirred at −78° C. for 15 minutes. Acetoxyacetyl chloride (2.3 ml) was injected and the mixture was stirred for 1 hour and then allowed to warm to room temperature. The reaction was quenched with 1N HCl and the product was extracted with diethyl ether (200 ml). The organic layer was dried, concentrated and recrystallized from ether/hexanes, yielding ethyl 4-(2,4-dichlorophenyl)-2,4-diketobutyrate (intermediate 1).

後処理

  1. stirringthe mixture was stirred for 1 hour
  2. temperatureto warm to room temperature
  3. customThe reaction was quenched with 1N HCl
  4. extractionthe product was extracted with diethyl ether (200 ml)
  5. customThe organic layer was dried
  6. concentrationconcentrated
  7. customrecrystallized from ether/hexanes

出典と根拠

ORDレコード
ord-c18014cf62e6472a80820d149fbcfe83
出典データセット
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06613777B1

反応ノート

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