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

HRID 631465
ノート
印刷プレビュー

反応式

HRID 631465 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 14798Sodium Hydroxide2 回HCID 159255Hydroxylamine, sulfate (1:1)HCID 866535185-Fluoro-4-(fluoromethyl)-4-methyl-3-oxopentanenitrile

生成物 1

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

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
HCID 962
Water
溶媒
2 回

反応条件

温度
100 °C

実験手順

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)+.

後処理

  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

出典と根拠

ORDレコード
ord-6787919b01a14f5dbdb7f5f794a20569
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09320739B2

反応ノート

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