Diethyl Malonate → Diethyl 2-(3-nitropyridin-4-yl)malonate

HRID 2414726ノート

反応式

HRID 2414726 の反応式
[H-].[Na+].[C:3]([O:11][CH2:12][CH3:13])(=[O:10])[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6].Cl[C:15]1[CH:20]=[CH:19][N:18]=[CH:17][C:16]=1[N+:21]([O-:23])=[O:22]>C1(C)C=CC=CC=1>[CH2:12]([O:11][C:3](=[O:10])[CH:4]([C:15]1[CH:20]=[CH:19][N:18]=[CH:17][C:16]=1[N+:21]([O-:23])=[O:22])[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH3:13]

参加物

5

反応物 3

HCID 7761Diethyl MalonateHCID 24758Sodium hydrideHCID 27357814-Chloro-3-nitropyridine

生成物 1

HCID 12244207Diethyl 2-(3-nitropyridin-4-yl)malonate収率 18.2%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

実験手順

To a suspension of 3.05 g of 60% sodium hydride (76.0 mmol) in toluene (50 mL) in a 250 mL RB flask was added 12.2 g of diethyl malonate (76.0 mmol) dropwise. The reaction mixture was stirred for 30 min under nitrogen, and a solution of 10.8 g of 4-chloro-3-nitropyridine (prepared according to the procedure of Houston et al. J. Med. Chem. 1985, 28, 467) in toluene (50 mL) was added dropwise and the resulting mixture refluxed for 4 h. The reaction mixture was concentrate, and the residue was partitioned between 100 mL each of dilute hydrochloric acid and diethyl ether. The aqueous phase was extracted twice with 100 mL of ether, and the combined ether phases were dried over magnesium sulfate and concentrated to give a dark oil. This was chromatographed on silica gel eluting With a hexane-30% hexane/EtOAc gradient to give 3.5 g of the title compound as a colorless oil which crystallized on standing. 1H NMR (DMSO-d6): δ 1.15 (t, J=7.1 Hz, 6H), 4.16 (q, J=7.1 Hz, 4H), 5.55 (s, 1H), 7.59 (d, J=5.1 Hz, 1H), 8.89 (d, J=5.1 Hz, 1H), 9.24 (s, 1H); C12H14N2O6: APES−MS m/z 281 (M−H).

後処理

  1. temperaturethe resulting mixture refluxed for 4 h
  2. concentrationThe reaction mixture was concentrate
  3. customthe residue was partitioned between 100 mL each of dilute hydrochloric acid and diethyl ether
  4. extractionThe aqueous phase was extracted twice with 100 mL of ether
  5. dry with materialthe combined ether phases were dried over magnesium sulfate
  6. concentrationconcentrated
  7. customto give a dark oil
  8. customThis was chromatographed on silica gel eluting With a hexane-30% hexane/EtOAc gradient

出典と根拠

ORDレコード
ord-974a4f29d021482092850373ecf69962
出典データセット
uspto-grants-2004_11
特許番号
US06815439B2

反応ノート

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