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Diethyl Oxalate → Ethyl 2-pyridineglyoxylate

HRID 278254
ノート
印刷プレビュー

反応式

HRID 278254 の反応式
C([Li])CCC.Br[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1.[C:13](OCC)(=[O:19])[C:14]([O:16][CH2:17][CH3:18])=[O:15]>CCOCC>[O:19]=[C:13]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1)[C:14]([O:16][CH2:17][CH3:18])=[O:15]
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 7268Diethyl OxalateHCID 79732-BromopyridineHCID 178418339Butyllithium

生成物 1

HCID 9989820Ethyl 2-pyridineglyoxylate

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

A solution of n-butyl lithium (100 mL, 1.6 M, 160 mmol) in hexanes was added over 2 min. to a stirred solution of 2-bromopyridine (15.0 mL, 24.9 g, 157 mmol) in 500 mL of ether cooled in a dry ice/isopropanol bath, causing a temporary rise in temperature to −47° C. After 25 min., the solution was transferred rapidly to a stirred 0° C. solution of diethyl oxalate (75 mL, 81 g, 550 mmol) in 1000 mL of ether. After 2 h at 0° C., the mixture was washed with saturated aq. sodium bicarbonate (900 mL), water (900 mL), and saturated aq. brine (450 mL). The organic layer was dried (magnesium sulfate), filtered, and evaporated. Distillation gave the title compound as 11.68 g of yellow liquid, B.p. 96-108° C. (0.3 mm Hg pressure). For the title compound:

後処理

  1. temperaturecooled in a dry ice/isopropanol bath
  2. customto −47° C
  3. customwas transferred rapidly to a stirred 0° C.
  4. waitAfter 2 h at 0° C.
  5. washthe mixture was washed with saturated aq. sodium bicarbonate (900 mL), water (900 mL), and saturated aq. brine (450 mL)
  6. dry with materialThe organic layer was dried (magnesium sulfate)
  7. filtrationfiltered
  8. customevaporated
  9. distillationDistillation

出典と根拠

ORDレコード
ord-8c8eeff692db41d189acd3244fe3eb7e
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06358979B1

反応ノート

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