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3-Bromo-1,1,1-trifluoro-2-propanone → Ethyl 4-(trifluoromethyl)thiazole-2-carboxylate

HRID 1497398
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HRID 1497398 반응식
[NH2:1][C:2](=[S:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4].Br[CH2:10][C:11](=O)[C:12]([F:15])([F:14])[F:13]>C(O)C>[F:13][C:12]([F:15])([F:14])[C:11]1[N:1]=[C:2]([C:3]([O:5][CH2:6][CH3:7])=[O:4])[S:8][CH:10]=1
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참가 물질

4

반응물 2

HCID 790083-Bromo-1,1,1-trifluoro-2-propanoneHCID 2733398Ethyl thiooxamate

생성물 1

HCID 23560697Ethyl 4-(trifluoromethyl)thiazole-2-carboxylate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of ethyl amino(thioxo)acetate (4 g) and 3-bromo-1,1,1-trifluoroacetone (3.1 ml) in ethanol (150 ml) was heated under reflux overnight. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate) to give the title compound (3.56 g).

후처리

  1. temperatureunder reflux overnight
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additionthe residue was diluted with water
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe obtained residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-952f4d1a092b4325a976f92b6c14a45f
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09199963B2

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