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4-Nitrobenzoyl chloride → 1-(4-Nitrophenyl)-1-propanone

HRID 1171036
ノート
印刷プレビュー

反応式

HRID 1171036 の反応式
[CH2:1]([Mg]Cl)[CH3:2].[N+:5]([C:8]1[CH:16]=[CH:15][C:11]([C:12](Cl)=[O:13])=[CH:10][CH:9]=1)([O-:7])=[O:6]>C1COCC1.O.[Cl-].[Cl-].[Zn+2].C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[N+:5]([C:8]1[CH:9]=[CH:10][C:11]([C:12](=[O:13])[CH2:1][CH3:2])=[CH:15][CH:16]=1)([O-:7])=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 2

HCID 85024-Nitrobenzoyl chlorideHCID 178461633HCID 178461633、化合物

生成物 1

HCID 947261-(4-Nitrophenyl)-1-propanone収率 40%

試薬・触媒・溶媒 4

HCID 3007855Zincchloride触媒HCID 178418397HCID 178418397、化合物触媒HCID 962
Water
溶媒
HCID 8028Tetrahydrofuran溶媒4 回

実験手順

A solution of 0.5M ZnCl2 in THF (60 mL, 30 mmol) in THF (20 mL) at room temperature was treated with 2M ethyl magnesium chloride in THF (15 mL, 30 mmol) dropwise via syringe, cooled with an ice bath for about 10 minutes, stirred at room temperature for 20 minutes, cooled to 0° C., and treated sequentially with Pd(PPh3)4 (1.73 g, 1.5 mmol) and a solution of 4-nitrobenzoyl chloride (6.12 g, 33 mmol) in THF (20 mL). The mixture was stirred at 0° C. for 40 minutes, diluted with water and extracted three times with ethyl acetate. The combined extracts were washed with saturated Na2CO3, water, and brine, dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 6:1 hexanes/ethyl acetate to provide 2.17 g (40%) of the desired product. Rf=0.6 (3:1 hexanes/ethyl acetate).

後処理

  1. temperaturecooled with an ice bath for about 10 minutes
  2. temperaturecooled to 0° C.
  3. stirringThe mixture was stirred at 0° C. for 40 minutes
  4. extractionextracted three times with ethyl acetate
  5. washThe combined extracts were washed with saturated Na2CO3, water, and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe concentrate was purified by flash column chromatography on silica gel with 6:1 hexanes/ethyl acetate

出典と根拠

ORDレコード
ord-314e5893ca454ed191fc01d7482381b3
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07829570B2

反応ノート

読み込み中…

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