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Diethyl Oxalate → HCID 86619018、化合物

HRID 1821803
ノート
印刷プレビュー

反応式

HRID 1821803 の反応式
[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]
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 3453632-Chloro-4-methyl-3-nitropyridineHCID 23670592Potassium ethoxide

生成物 1

HCID 86619018HCID 86619018、化合物収率 81.6%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-b9ac46418dce47f389fdb4613caa8cdd
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07608627B2

反応ノート

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