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D-Glutamic Acid → (R)-5-oxo-2-tetrahydrofurancarboxylic acid

HRID 500345
ノート
印刷プレビュー

反応式

HRID 500345 の反応式
N[C@@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][C:5]([OH:7])=[O:6].N([O-])=O.[Na+]>O.Cl>[O:9]=[C:8]1[O:10][C@@H:4]([C:5]([OH:7])=[O:6])[CH2:3][CH2:2]1
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 2

HCID 23327D-Glutamic AcidHCID 23668193Sodium Nitrite

生成物 1

HCID 104532(R)-5-oxo-2-tetrahydrofurancarboxylic acid収率 57.1%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 962Water溶媒2 回

実験手順

To a mixture of D-glutamic acid (1, 25 g, 170 mmol) in water (67 mL) and conc. HCl (35 mL) at 0° C. with stirring was added a solution of NaNO2 (17.5 g, 253.6 mmol) in water (37.5 mL) over a period of 4 h, and then the resulting clear solution was stirred at room temperature overnight. After removal of the solvent by evaporation in vacuo, the residue was treated with EtOAC (80 mL) and filtered. The filtrate was dried over Na2SO4, and concentrated. The residue, after crystallization from EtOAc/benzene/hexane, afforded the title compound 2 as a white crystalline solid (12.63 g, 57%). M.P. 71-73° C.; 1H NMR (400 MHz, CD3OD) δ 4.20 (m, 1H, CHO), 1.8-2.3 (m, 4H, CH2CH2).

後処理

  1. stirringthe resulting clear solution was stirred at room temperature overnight
  2. customAfter removal of the solvent
  3. customby evaporation in vacuo
  4. additionthe residue was treated with EtOAC (80 mL)
  5. filtrationfiltered
  6. dry with materialThe filtrate was dried over Na2SO4
  7. concentrationconcentrated
  8. customThe residue, after crystallization from EtOAc/benzene/hexane

出典と根拠

ORDレコード
ord-bc4cc98b77dc4eb39a46e3f8a01cd65c
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07772208B2

反応ノート

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