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Sodium Hydroxide → 3-(1,3-Difluoro-2-methylpropan-2-yl)isoxazol-5-amine

HRID 631465
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HRID 631465 반응식
[F:1][CH2:2][C:3]([CH2:10][F:11])([CH3:9])[C:4](=O)[CH2:5][C:6]#[N:7].[OH-:12].[Na+].S(O)(O)(=O)=O.[NH2:19]O>CCO.O>[F:1][CH2:2][C:3]([C:4]1[CH:5]=[C:6]([NH2:7])[O:12][N:19]=1)([CH3:9])[CH2:10][F:11]
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참가 물질

6

반응물 3

HCID 14798Sodium Hydroxide2회HCID 159255Hydroxylamine, sulfate (1:1)HCID 866535185-Fluoro-4-(fluoromethyl)-4-methyl-3-oxopentanenitrile

생성물 1

HCID 668767503-(1,3-Difluoro-2-methylpropan-2-yl)isoxazol-5-amine수율 17.5%

시약·촉매·용매 2

HCID 702Ethanol용매
HCID 962
Water
용매
2회

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온도
100 °C

실험 절차

To a solution of 5-fluoro-4-(fluoromethyl)-4-methyl-3-oxopentanenitrile (1.00 g, 6.2 mmol) and NaOH (0.272 g, 6.8 mmol) in EtOH (5 mL) and water (5 mL) at room temperature was added a solution of hydroxylamine sulfate (1.12 g, 6.8 mmol) in water (5 mL). To the mixture was added additional NaOH until the pH was about 8. After heating at 100° C. for 2 hours, it was quenched with water and extracted with CH2Cl2. Extracts were washed with water, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluted with with gradient of 0-50% EtOAc/hexane to afford 3-(1,3-difluoro-2-methylpropan-2-yl)isoxazol-5-amine as a solid (0.191 g, 17%). 1H NMR (300 MHz, CDCl3) δ 5.16 (s, 1H), 4.63 (q, 2H), 4.5 (q and br, 4H), 1.37 (s, 3H); LC-MS (ESI) m/z 177 (M+H)+.

후처리

  1. customit was quenched with water
  2. extractionextracted with CH2Cl2
  3. washExtracts were washed with water
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel chromatography
  7. washeluted with with gradient of 0-50% EtOAc/hexane

출처 및 근거

ORD 기록
ord-6787919b01a14f5dbdb7f5f794a20569
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09320739B2

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