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Trifluoroacetic acid → HCID 90389354, 화합물

HRID 1526538
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HRID 1526538 반응식
[F:1][CH:2]([F:17])[C:3]1([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([F:15])[C:10]=2[CH3:16])[CH:8]2[CH:6]([CH2:7]2)[O:5][NH:4]1.FC(F)(F)C(O)=O>C(O)(=O)C.[Zn]>[NH2:4][C:3]([CH:8]1[CH2:7][CH:6]1[OH:5])([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([F:15])[C:10]=1[CH3:16])[CH:2]([F:1])[F:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6422Trifluoroacetic acidHCID 90389378HCID 90389378, 화합물

생성물 1

HCID 90389354HCID 90389354, 화합물수율 74.7%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

To a solution of 4-(difluoromethyl)-4-(3-fluoro-2-methylphenyl)-2-oxa-3-azabicyclo[3.1.0]hexane (0.81 g, 3.33 mmol) in acetic acid, glacial (7.69 ml, 133 mmol) was added zinc (1.306 g, 19.98 mmol) portionwise at RT followed by trifluoroacetic acid (2.474 ml, 33.3 mmol). The reaction was stirred at RT for 1 hour. The reaction was filtered through a pad of celite and concentrated under vacuum. The residue was dissolved in iced water and the solution was basified by the addition of 5N NaOH to pH 12. The basic aqueous layer was back extracted with EtOAc. The organic layer was washed with brine, dried over sodium sulfate, and concentrated to dryness to afford the title compound 2-(1-amino-2,2-difluoro-1-(3-fluoro-2-methylphenyl)ethyl)cyclopropanol (0.61 g, 2.487 mmol, 74.7% yield). LC/MS (ESI+) m/z=246.1 (M+H).

후처리

  1. filtrationThe reaction was filtered through a pad of celite
  2. concentrationconcentrated under vacuum
  3. dissolutionThe residue was dissolved in iced water
  4. additionthe solution was basified by the addition of 5N NaOH to pH 12
  5. extractionThe basic aqueous layer was back extracted with EtOAc
  6. washThe organic layer was washed with brine
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-c30df3f811764d42a7fd43ee98a61527
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085576B2

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