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Sodium Hydroxide → 1-(3-(Hydroxymethyl)isoxazol-5-yl)ethanone

HRID 416276
ノート
印刷プレビュー

反応式

HRID 416276 の反応式
[CH3:1][C:2]1([C:7]2[O:11][N:10]=[C:9]([CH2:12][OH:13])[CH:8]=2)OCC[O:3]1.[OH-].[Na+]>CO>[OH:13][CH2:12][C:9]1[CH:8]=[C:7]([C:2](=[O:3])[CH3:1])[O:11][N:10]=1
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

4

反応物 2

HCID 14798Sodium HydroxideHCID 58930623(5-(2-Methyl-1,3-dioxolan-2-yl)isoxazol-3-yl)methanol

生成物 1

HCID 589304951-(3-(Hydroxymethyl)isoxazol-5-yl)ethanone収率 92%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
70 °C

実験手順

To a solution of the carbinol 319 (2.39 g, 12.9 mmol) in MeOH (30 mL) 10% HCl (30 mL) was added. The reaction mixture was stirred at 70° C. for 18 hours, cooled and neutralized to pH 6 using 1M NaOH solution. MeOH was evaporated and the resulting aqueous phase was extracted with EtOAc. The organic layer was washed with brine, dried under MgSO4 and concentrated under reduced pressure to produce the title compound as a beige solid (1.67 g, 92% yield), which was used for next step without further purification. 1H NMR (DMSO-d6) δ (ppm): 7.25 (s, 1H), 5.62 (t, J=6.1 Hz, 1H), 4.56 (d, J=5.9 Hz, 2H), 2.56 (s, 3H). MS (m/z): 141.12 (calc) 142.1 (MH+) (found)

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturecooled and neutralized to pH 6
  2. customMeOH was evaporated
  3. extractionthe resulting aqueous phase was extracted with EtOAc
  4. washThe organic layer was washed with brine
  5. customdried under MgSO4
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-13188c699154478db703bb4a70f45bd8
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08088805B2

反応ノート

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