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Diethyl Oxalate → HCID 86619018, 화합물

HRID 1821803
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HRID 1821803 반응식
[O-]CC.[K+:4].[C:5]([O:12][CH2:13][CH3:14])(=[O:11])[C:6]([O:8]CC)=O.[Cl:15][C:16]1[C:21]([N+:22]([O-:24])=[O:23])=[C:20]([CH3:25])[CH:19]=[CH:18][N:17]=1>C(OCC)C>[Cl:15][C:16]1[C:21]([N+:22]([O-:24])=[O:23])=[C:20](/[CH:25]=[C:6](\[O-:8])/[C:5]([O:12][CH2:13][CH3:14])=[O:11])[CH:19]=[CH:18][N:17]=1.[K+:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7268Diethyl OxalateHCID 3453632-Chloro-4-methyl-3-nitropyridineHCID 23670592Potassium ethoxide

생성물 1

HCID 86619018HCID 86619018, 화합물수율 81.6%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a heterogeneous solution of potassium ethoxide (6.56 g, 77.9 mmol) in diethyl ether (55 mL), was slowly added diethyl oxalate (10.6 mL, 77.9 mmol). A slight exotherm resulted. After stirring 5 min, a homogeneous yellow solution resulted, but after 10 min, a heterogeneous yellow slurry was observed. Addition of 2-chloro-4-methyl-3-nitropyridine (13.45 g, 77.9 mmol) as a solid, with a diethyl ether rinse (23 mL), resulted in a dark violet solution with a dark precipitate. The mixture was stirred at room temperature overnight (21 h). The solid precipitate was filtered, rinsed thoroughly with diethyl ether, and air-dried to give potassium (1Z)-1-(2-chloro-3-nitropyridin-4-yl)-3-ethoxy-3-oxoprop-1-en-2-olate (19.8 g, 63.6 mmol, yield 81%) as an orange solid. The crude product was used directly without further purification or identification.

후처리

  1. customA slight exotherm resulted
  2. customa homogeneous yellow solution resulted
  3. waitafter 10 min
  4. washwith a diethyl ether rinse (23 mL)
  5. customresulted in a dark violet solution with a dark precipitate
  6. stirringThe mixture was stirred at room temperature overnight (21 h)
  7. filtrationThe solid precipitate was filtered
  8. washrinsed thoroughly with diethyl ether
  9. customair-dried

출처 및 근거

ORD 기록
ord-b9ac46418dce47f389fdb4613caa8cdd
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07608627B2

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