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Ethyl 4,4,4-trifluoroacetoacetate → HCID 178472917, 화합물

HRID 1492495
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인쇄 미리보기

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HRID 1492495 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

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

생성물 1

HCID 178472917HCID 178472917, 화합물

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

반응 조건

온도
15 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-a853ad9a1e5d49d9b9ca800d8fdc2d4b
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05374615

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