Ammonium Chloride → Diethyl 5-ethylpyridine-2,3-dicarboxylate

HRID 742203

반응식

HRID 742203 반응식
C(O[CH:4]=[C:5]([C:11]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=O)[C:6]([O:8][CH2:9][CH3:10])=[O:7])C.O1CC[N:21]([CH:24]=[CH:25][CH2:26][CH3:27])CC1.[NH4+].[Cl-]>CO.C(O)(=O)C>[CH2:26]([C:25]1[CH:4]=[C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])[C:11]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[N:21][CH:24]=1)[CH3:27]

참가 물질

6

반응물 3

HCID 25517Ammonium ChlorideHCID 40590Diethyl 2-(ethoxymethylidene)-3-oxobutanedioateHCID 5809771-Morpholinobutene

생성물 1

HCID 10857926Diethyl 5-ethylpyridine-2,3-dicarboxylate

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 887Methanol용매

실험 절차

To a solution of diethyl ethoxymethyleneoxalacetate (43.2 g, 0.16 mol) dissolved in CH3OH (150 mL) at -10° under N2 is added 1-morpholinobutene (25 g, 0.16 mol). The reaction is slowly warmed to room temperature over three hours, after which the CH3OH is removed in vacuo. The residue is dissolved in acetic acid (100 mL) and this solution slowly added to NH4Cl (34.2 g, 0.64 mol) dissolved in acetic acid (200 mL) at 50°-70°. The reaction is then heated to 90°-95° for two hours and 30 minutes, concentrated in vacuo, partitioned between water and the CH2Cl2, and the organic phase chromatographed over silica gel with CH2Cl2 --CH3CN (95:5) elution to give the product as an oil. Distillation at 123°-155° at 0.15 mm gives the product (23.4 g, 83% pure, 55%).

후처리

  1. customafter which the CH3OH is removed in vacuo
  2. dissolutionThe residue is dissolved in acetic acid (100 mL)
  3. temperatureThe reaction is then heated to 90°-95° for two hours and 30 minutes
  4. concentrationconcentrated in vacuo
  5. custompartitioned between water
  6. customthe CH2Cl2, and the organic phase chromatographed over silica gel with CH2Cl2 --CH3CN (95:5) elution

출처 및 근거

ORD 기록
ord-9c4e9098250441b298de33a0ad2f23cb
출처 데이터셋
uspto-grants-1996_09
특허 번호
US05554579

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