Potassium Iodide → Methyl (m-[m-phenoxyphenoxy]phenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate

HRID 1704041Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1704041
[O:1]([C:8]1[CH:9]=[C:10]([CH:19]=[CH:20][CH:21]=1)[O:11][C:12]1[CH:13]=[C:14]([OH:18])[CH:15]=[CH:16][CH:17]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[O-].[Na+].[I-].[K+].Br[CH:28]([C:33]1[CH:38]=[CH:37][C:36]([O:39][C:40]2[CH:45]=[CH:44][C:43]([Cl:46])=[CH:42][CH:41]=2)=[CH:35][CH:34]=1)[C:29]([O:31][CH3:32])=[O:30]>CO.C1C=CC=CC=1.O>[CH3:32][O:31][C:29](=[O:30])[CH:28]([O:18][C:14]1[CH:15]=[CH:16][CH:17]=[C:12]([O:11][C:10]2[CH:19]=[CH:20][CH:21]=[C:8]([O:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH:9]=2)[CH:13]=1)[C:33]1[CH:34]=[CH:35][C:36]([O:39][C:40]2[CH:45]=[CH:44][C:43]([Cl:46])=[CH:42][CH:41]=2)=[CH:37][CH:38]=1

Komponenten

8

Versuchsvorschrift

To a solution of 6.96 g of m-(m-phenoxyphenoxy)phenol, 1.19 g of sodium methoxide and 50 mg of potassium iodide in 40 ml of methanol is added 7.11 g of methyl α-bromo-α-(p-(p-chlorophenoxy)phenyl]acetate in 10 ml of benzene. The mixture is refluxed for 20 hours, poured into ice and water and extracted with chloroform. The chloroform extracts are washed with 10% potassium carbonate and with water. The extract is dried over magnesium sulfate and concentrated under vacuum to given an oil. Filtration once through silica gel (chloroform solvent) and again through silica gel with benzene as solvent gives the product as an oil.

Aufarbeitung

  1. temperatureThe mixture is refluxed for 20 hours
  2. extractionextracted with chloroform
  3. washThe chloroform extracts are washed with 10% potassium carbonate and with water
  4. dry with materialThe extract is dried over magnesium sulfate
  5. concentrationconcentrated under vacuum
  6. filtrationFiltration once through silica gel (chloroform solvent)

Quellen und Nachweise

ORD-Eintrag
ord-4a260825f16c41b28a46b486012bb71e
Quelldatensatz
uspto-grants-1978_11
Patentnummer
US04125729

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