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Sodium Carbonate → HCID 58305608、化合物

HRID 2280277
ノート
印刷プレビュー

反応式

HRID 2280277 の反応式
O=P(Cl)(Cl)Cl.[CH3:6][C:7]1[CH:8]=[C:9]([CH:13]=[CH:14][C:15]=1[N:16]1[CH:20]=[CH:19][CH:18]=[CH:17]1)[C:10]([NH2:12])=O.[C:21]([O-])([O-])=[O:22].[Na+].[Na+]>CN(C=O)C>[CH:21]([C:17]1[N:16]([C:15]2[CH:14]=[CH:13][C:9]([C:10]#[N:12])=[CH:8][C:7]=2[CH3:6])[CH:20]=[CH:19][CH:18]=1)=[O:22]
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 10340Sodium CarbonateHCID 24813Phosphorus oxychlorideHCID 58305652HCID 58305652、化合物

生成物 1

HCID 58305608HCID 58305608、化合物収率 68%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

POCl3 (65 g, 427 mmol) was added to DMF (34 mL) at 0° C. for 30 min. After addition, the mixture was stirred at room temperature for 1.5 h, and then cooled to 0° C. A solution of 3-methyl-4-(1H-pyrrol-1-yl)benzamide (6A) (42.7 g, 213.5 mmol) in DMF (150 mL) was added at 0° C. and the resultant mixture was stirred at room temperature for 20 min, and then heated to 80° C. for 1 h. The solution was cooled to room temperature and then sat. Na2CO3 was added at 0° C. until pH=8. The mixture was extracted with ethyl acetate three times. The combined organic layers were washed with sat. NaHCO3 and brine, dried over Na2SO4, concentrated and purified by silica gel column chromatography (PE:EA=10:1) to afford 4-(2-formyl-1H-pyrrol-1-yl)-3-methylbenzonitrile as a yellow solid (30.5 g, yield 68%).

後処理

  1. additionAfter addition
  2. temperaturecooled to 0° C
  3. temperatureheated to 80° C. for 1 h
  4. temperatureThe solution was cooled to room temperature
  5. extractionThe mixture was extracted with ethyl acetate three times
  6. washThe combined organic layers were washed with sat. NaHCO3 and brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated
  9. custompurified by silica gel column chromatography (PE:EA=10:1)

出典と根拠

ORDレコード
ord-b7bc37e65c7f4c298af3c319f81f1aae
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09138427B2

反応ノート

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