Pyrrole → 4,5-Dichloro-2-(3,4-dichlorophenyl)-1-(2-hydroxyethyl)-pyrrole-2-carbonitrile

HRID 1085603

反応式

HRID 1085603 の反応式
[Cl:1][C:2]1[C:3](C#N)=[C:4]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[C:10]([Cl:15])[CH:9]=2)[NH:5][C:6]=1[Cl:7].[CH3:18][C:19](C)([O-:21])C.[K+].BrC(O)C.[NH:28]1C=CC=[CH:29]1>O1CCOCC1.O.C(OCC)(=O)C>[Cl:1][C:2]1[CH2:3][C:4]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[C:10]([Cl:15])[CH:9]=2)([C:29]#[N:28])[N:5]([CH2:18][CH2:19][OH:21])[C:6]=1[Cl:7]

参加物

8

実験手順

To a stirred mixture of 2.0 g (6.5 mmol) of 4,5-dichloro-2-(3,4-dichlorophenyl)-pyrrole-3-carbonitrile and 0.88 g (7.8 mmol) of potassium tert-butoxide heated at reflux in 50 mL of dioxane is added 0.98 g (7.8 mmol) of bromoethanol. The mixture is stirred at reflux for 12 hours, cooled, diluted with 50 mL of water, and extracted several times with chloroform. The combined chloroform extracts are dried over magnesium sulfate and concentrated in vacuo to leave a solid which, on warming and dissolving in ethyl acetate, deposits on cooling mostly starting pyrrole. Concentration of the mother liquor and recrystallization of the residual solid from 20% ethyl acetate in hexane gives 0.31 g of a white solid, mp 143°-145° C.; IR 5077A.

後処理

  1. temperatureheated
  2. temperatureat reflux for 12 hours
  3. temperaturecooled
  4. extractionextracted several times with chloroform
  5. dry with materialThe combined chloroform extracts are dried over magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. customto leave a solid which
  8. temperatureon warming
  9. customConcentration of the mother liquor and recrystallization of the residual solid from 20% ethyl acetate in hexane

出典と根拠

ORDレコード
ord-7c6a8238d4b340fea450e95059ce81ba
出典データセット
uspto-grants-1991_04
特許番号
US05010098

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