Carbon Dioxide → 4-(2-Tetrahydropyranyloxyethoxy)benzoic acid

HRID 1659621Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1659621
[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH2:9][O:10][C:11]1[CH:16]=[CH:15][C:14](Br)=[CH:13][CH:12]=1.[Mg].[C:19](=[O:21])=[O:20]>O1CCCC1>[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH2:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([C:19]([OH:21])=[O:20])=[CH:13][CH:12]=1

Komponenten

5

Edukt 3

HCID 280Carbon DioxideHCID 5462224Magnesium2×HCID 128104732-[2-(4-Bromophenoxy)ethoxy]tetrahydro-2H-pyran

Produkt 1

HCID 128104744-(2-Tetrahydropyranyloxyethoxy)benzoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel3×

Versuchsvorschrift

A mixture of 9.45 g (31.4 mmol) of 4-(2-tetrahydropyranyloxyethoxy)bromobenzene, 40 ml of dry tetrahydrofuran (THF) and 0.76 g (31.4 mmol) of magnesium metal is heated to boiling, and after about 15 minutes a spontaneous reaction ensues. The mixture is then maintained, with some external heating, at its boiling point and after 15 minutes 20 ml of THF is added. After an additional 15 minutes at boiling, a final 20 ml of THF is added, and boiling is continued until the total heating time is 2 hours. Most of the magnesium has disappeared at this point. The mixture is then cooled and carbon dioxide gas is introduced, at a slight positive pressure and with vigorous stirring, for 15 minutes. The mixture is filtered and rotoevaporated to remove the solvent. Ethyl acetate (150 ml), water (150 ml) and aqueous 3 N sulfuric acid (20 ml) are added to the residue. The aqueous layer is separated and extracted with ethyl acetate. The combined organic layers are washed with water (100 ml, 2×) and then with saturated aqueous sodium chloride and dried over calcium sulfate. Solvent is removed by rotoevaporation to give 4-(2-tetrahydropyranyloxyethoxy)benzoic acid.

Aufarbeitung

  1. temperatureis heated
  2. customafter about 15 minutes a spontaneous reaction
  3. additionis added
  4. waitis 2 hours
  5. temperatureThe mixture is then cooled
  6. filtrationThe mixture is filtered
  7. customto remove the solvent
  8. additionEthyl acetate (150 ml), water (150 ml) and aqueous 3 N sulfuric acid (20 ml) are added to the residue
  9. customThe aqueous layer is separated
  10. extractionextracted with ethyl acetate
  11. washThe combined organic layers are washed with water (100 ml, 2×)
  12. dry with materialwith saturated aqueous sodium chloride and dried over calcium sulfate
  13. customSolvent is removed by rotoevaporation

Quellen und Nachweise

ORD-Eintrag
ord-ef0045b8e14d4cf6912396e112e68a10
Quelldatensatz
uspto-grants-1981_12
Patentnummer
US04304924

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