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Ethyl Acetate → methyl 2-(5-bromo-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetate

HRID 1471656
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HRID 1471656 반응식
[Br:1][C:2]1[NH:6][N:5]=[C:4]([C:7]([F:10])([F:9])[F:8])[CH:3]=1.C([O-])([O-])=O.[Cs+].[Cs+].Br[CH2:18][C:19]([O:21][CH3:22])=[O:20].C(OCC)(=O)C>C(#N)C.O>[Br:1][C:2]1[N:6]([CH2:18][C:19]([O:21][CH3:22])=[O:20])[N:5]=[C:4]([C:7]([F:10])([F:9])[F:8])[CH:3]=1
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참가 물질

7

반응물 4

HCID 8857Ethyl AcetateHCID 10796Cesium carbonateHCID 60984Methyl bromoacetateHCID 178506065HCID 178506065, 화합물

생성물 1

HCID 90281248methyl 2-(5-bromo-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetate수율 32%

시약·촉매·용매 2

HCID 962Water용매
HCID 6342Acetonitrile용매

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온도
80 °C

실험 절차

To a solution of 5-bromo-3-(trifluoromethyl)-1H-pyrazole (1.0 g, 4.6 mmol) and Cs2CO3 (3.0 g, 9.3 mmol) in acetonitrile (10 mL) was added methyl 2-bromoacetate (865 mg, 5.6 mmol). The reaction was heated at 80° C. for 3 h. After the reaction was cooled to room temperature, the mixture was portioned between ethyl acetate and water. The organic layer was separated and washed with saturated aqueous NH4Cl and brine. The organic layer was then dried over Na2SO4, filtered and concentrated to afford crude product which was purified by silica gel chromatography eluting with dichloromethane/hexanes to afford methyl 2-(5-bromo-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetate (420 mg, 32%) as a clear oil. MS (m/z): 287.1 [M+H]+; HPLC retention time 2.93 min (2-98% acetonitrile:water with 0.05% trifluoroacetic acid).

후처리

  1. temperatureAfter the reaction was cooled to room temperature
  2. customThe organic layer was separated
  3. washwashed with saturated aqueous NH4Cl and brine
  4. dry with materialThe organic layer was then dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto afford crude product which
  8. customwas purified by silica gel chromatography
  9. washeluting with dichloromethane/hexanes

출처 및 근거

ORD 기록
ord-03961bc40d9940fc8d13b33503fa1bd2
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012441B2

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