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2,2,2-Trifluoroethanol → HCID 89874843, 화합물

HRID 715427
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HRID 715427 반응식
Cl[C:2]1[N:3]=[CH:4][C:5]([C:9]([O:11][CH3:12])=[O:10])=[N:6][C:7]=1[CH3:8].[F:13][C:14]([F:18])([F:17])[CH2:15][OH:16].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[CH3:8][C:7]1[N:6]=[C:5]([C:9]([O:11][CH3:12])=[O:10])[CH:4]=[N:3][C:2]=1[O:16][CH2:15][C:14]([F:18])([F:17])[F:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 64092,2,2-TrifluoroethanolHCID 11430Potassium CarbonateHCID 12619146Methyl 5-chloro-6-methylpyrazine-2-carboxylate

생성물 1

HCID 89874843HCID 89874843, 화합물수율 97.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
60 °C

실험 절차

A mixture of methyl 5-chloro-6-methylpyrazine-2-carboxylate (3.00 g, 16.1 mmol), 2,2,2-trifluoroethanol (32.2 g, 322 mmol), and potassium carbonate (3.33 g, 24.1 mmol) in DMF (30 mL) is stirred at 60° C. for 2 hours. After cooling to rt, the mixture is filtered off, and the filtrate is diluted with EtOAc (300 mL). The organic layer is washed with water (100 mL×3) and dried over sodium sulfate. After filtration, the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting EtOAc to give 3.91 g (97% yield) of the title compound as white solid.

후처리

  1. temperatureAfter cooling to rt
  2. filtrationthe mixture is filtered off
  3. additionthe filtrate is diluted with EtOAc (300 mL)
  4. washThe organic layer is washed with water (100 mL×3)
  5. dry with materialdried over sodium sulfate
  6. filtrationAfter filtration
  7. concentrationthe filtrate is concentrated in vacuo
  8. customThe residue is purified by column chromatography on silica gel
  9. washeluting EtOAc

출처 및 근거

ORD 기록
ord-73656ca36af74fd4bd130d921426ff79
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187475B2

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