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Tetrahydrofuran → (S)-2-(2-Oxo-2H-pyridin-1-yl)-propionic acid

HRID 419678
ノート
印刷プレビュー

反応式

HRID 419678 の反応式
C([O:3][C:4](=[O:14])[C@@H:5]([N:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]1=[O:13])[CH3:6])C.C1COCC1.[OH-].[Na+]>O>[O:13]=[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][N:7]1[C@@H:5]([CH3:6])[C:4]([OH:14])=[O:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 66650045(S)-2-(2-Oxo-2H-pyrid-1-yl)-propionic acid ethyl ester

生成物 1

HCID 53628857(S)-2-(2-Oxo-2H-pyridin-1-yl)-propionic acid収率 27%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A stirred mixture of (S)-2-(2-Oxo-2H-pyrid-1-yl)-propionic acid ethyl ester (364 mg, 1.87 mmol), THF (2 ml), water (1 ml) and sodium hydroxide (90 mg, 2.24 mmol) was kept at room temperature for 1 h, then concentrated under reduced pressure. The residue was dissolved in ether and the resulting solution washed with water. The organic layer was discarded and the aqueous layer was acidified with concentrated HCl then extracted several times with ethyl acetate. The combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was triturated with ether to afford the title compound as a colorless solid (84 mg, 27%): [α]31D=−50° (c=0.2, CH3OH); 1H NMR (400 MHz, DMSO) δ 1.5 (3H, d), 5.1 (1H, q), 6.2 (1H, t), 6.4 (1H, d), 7.4 (1H, m), 7.6 (1H, d).

後処理

  1. concentrationconcentrated under reduced pressure
  2. dissolutionThe residue was dissolved in ether
  3. washthe resulting solution washed with water
  4. extractionthen extracted several times with ethyl acetate
  5. dry with materialThe combined organic extracts were dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was triturated with ether

出典と根拠

ORDレコード
ord-85745ad5bdfc47c0aa199427ac65b275
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08093392B2

反応ノート

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