Diethyl Ether → HCID 13067091、化合物

HRID 1903625ノート

反応式

HRID 1903625 の反応式
[Cl:1][C:2]1[CH:20]=[CH:19][CH:18]=[CH:17][C:3]=1[C:4]([C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][C:7]=1[CH:13]=[CH:14][C:15]#[N:16])=[O:5].S([CH:31]([N+:33]#[C-])C)(C1C=CC(C)=CC=1)(=O)=O.[H-].[Na+].[CH3:37][CH2:38]OCC>CS(C)=O.O.Cl>[Cl:12][C:10]1[CH:9]=[CH:8][C:7]([C:13]2[C:14]([C:31]#[N:33])=[CH:15][NH:16][C:37]=2[CH3:38])=[C:6]([C:4](=[O:5])[C:3]2[CH:17]=[CH:18][CH:19]=[CH:20][C:2]=2[Cl:1])[CH:11]=1

参加物

8

実験手順

A mixture of 33.9 g (0.11 mol) of 3-[2-(2-chlorobenzoyl)-4-chlorophenyl]-2-propenenitrile, 20 g (0.96 mol) of 1-tosylethyl isocyanide in 150 ml of dimethyl sulfoxide and 100 ml of ether was added dropwise to a suspension of 4.6 g (0.1 mol) of a 50% mineral oil dispension of sodium hydride in 100 ml of ether which was immersed in a room temperature water bath. Stirring at room temperature was continued for 2 hours. The mixture was diluted with 1.2 liters of water and 40 ml of 1 N hydrochloric acid and extracted with methylene chloride. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate and concentrated at reduced pressure to give a dark green oil. Crystallization from a mixture of ether and petroleum ether gave 4-[4-chloro-2-(2-chlorobenzoyl)phenyl]-5-methyl-1H-pyrrole-3-carbonitrile, mp 206°-208° C., as tan crystals. Recrystallization from ether gave the desired product as colorless crystals, mp 210°-211° C.

後処理

  1. customwas immersed in a room temperature
  2. extractionextracted with methylene chloride
  3. washThe methylene chloride solution was washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated at reduced pressure
  6. customto give a dark green oil
  7. customCrystallization
  8. additionfrom a mixture of ether and petroleum ether

出典と根拠

ORDレコード
ord-06f7cdc75247415681109a1bab991d1b
出典データセット
uspto-grants-1984_03
特許番号
US04436662

反応ノート

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