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Diethyl Oxalate → Ethyl 2-pyridineglyoxylate

HRID 278254
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HRID 278254 반응식
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]
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참가 물질

5

반응물 3

HCID 7268Diethyl OxalateHCID 79732-BromopyridineHCID 178418339Butyllithium

생성물 1

HCID 9989820Ethyl 2-pyridineglyoxylate

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

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:

후처리

  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

출처 및 근거

ORD 기록
ord-8c8eeff692db41d189acd3244fe3eb7e
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06358979B1

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