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Ethyl 4,4,4-trifluoroacetoacetate → HCID 178472917、化合物

HRID 1492495
ノート
印刷プレビュー

反応式

HRID 1492495 の反応式
[N:1]([O-:3])=O.[Na+].[F:5][C:6]([F:16])([F:15])[C:7](=[O:14])[CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10]>O.C(O)(=O)C>[F:5][C:6]([F:15])([F:16])[C:7](=[O:14])[C:8](=[N:1][OH:3])[C:9]([O:11][CH2:12][CH3:13])=[O:10]
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 2

HCID 67793Ethyl 4,4,4-trifluoroacetoacetateHCID 23668193Sodium Nitrite

生成物 1

HCID 178472917HCID 178472917、化合物

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 962Water溶媒

反応条件

温度
15 °C

実験手順

A solution of sodium nitrite (0.29 mmol) in 35 mL of water was added dropwise over 50 minutes to a stirred, ice-cooled solution of 22.8 g of ethyl 4,4,4-trifluoroacetoacetate (0.12 mmol) in 30 mL of acetic acid. The reaction was continued for 2 hours, with gradual warming to 15° C. Water and acetic acid were removed under reduced pressure (azeotroped with toluene). The crude product was partitioned between ethyl acetate and saturated aqueous potassium hydrogen carbonate solution. The layers were separated. The ethyl acetate layer was washed with saturated aqueous potassium hydrogen carbonate solution and brine, dried over sodium sulfate and concentrated to yield 21.4 g of the title A compound as a light yellow oil.

後処理

  1. customWater and acetic acid were removed under reduced pressure (azeotroped with toluene)
  2. customThe crude product was partitioned between ethyl acetate and saturated aqueous potassium hydrogen carbonate solution
  3. customThe layers were separated
  4. washThe ethyl acetate layer was washed with saturated aqueous potassium hydrogen carbonate solution and brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-a853ad9a1e5d49d9b9ca800d8fdc2d4b
出典データセット
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05374615

反応ノート

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