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Sodium hydride → HCID 178526672, 화합물

HRID 1289837
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HRID 1289837 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][N:11]=[C:12]([C:19]([F:22])([F:21])[F:20])[CH2:13][C:14](OCC)=[O:15])=[CH:6][CH:5]=1)([O-:3])=[O:2].[H-].[Na+]>C1COCC1>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[C:14]([OH:15])=[CH:13][C:12]([C:19]([F:22])([F:21])[F:20])=[N:11]2)=[CH:6][CH:5]=1)([O-:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24758Sodium hydrideHCID 2738115Ethyl trifluoroacetoacetate 4-nitrophenylhydrazone

생성물 1

HCID 178526672HCID 178526672, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
50 °C

실험 절차

To a mixture of 382 mg (1.2 mmol) of ethyl trifluoroacetoacetate 4-nitrophenylhydrazone in 10 ml of THF was added 53 mg (60%; 1.32 mmol) of NaH and the resulting mixture was stirred at room temperature for 4 hours and at 50° C. for 16 hours. The reaction mixture was quenched with ammonium chloride solution, the aqueous layer was extracted with ethyl acetate (3×), and the combined organic layer was dried and concentrated in vacuo. The residue was purified by column chromatography (silica gel; 50% ethyl acetate in hexane) and recrystallized from methylene chloride/hexane to afford 1-(4-nitrophenyl)-3-trifluoromethyl-5-hydroxypyrazole as a white solid.

후처리

  1. customThe reaction mixture was quenched with ammonium chloride solution
  2. extractionthe aqueous layer was extracted with ethyl acetate (3×)
  3. customthe combined organic layer was dried
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography (silica gel; 50% ethyl acetate in hexane)
  6. customrecrystallized from methylene chloride/hexane

출처 및 근거

ORD 기록
ord-1e1d1efa4c5d42c19763fdedab9c9907
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05750550

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