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Methanesulfonic Acid → Di-(4-tolyl)-4-octyloxyphenylsulfonium 10-camphorsulfonate

HRID 645330
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 645330
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.CS(O)(=O)=O.[CH2:20]([O:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27].[C:35]1([CH3:50])[CH:40]=[CH:39][C:38]([S:41]([C:43]2[CH:48]=[CH:47][C:46]([CH3:49])=[CH:45][CH:44]=2)=O)=[CH:37][CH:36]=1.[C:51]12([CH2:61][S:62]([O-:65])(=[O:64])=[O:63])[C:58]([CH3:60])([CH3:59])[CH:55]([CH2:56][CH2:57]1)[CH2:54][C:52]2=[O:53].[NH4+]>>[C:51]12([CH2:61][S:62]([O-:65])(=[O:63])=[O:64])[C:58]([CH3:60])([CH3:59])[CH:55]([CH2:56][CH2:57]1)[CH2:54][C:52]2=[O:53].[C:46]1([CH3:49])[CH:45]=[CH:44][C:43]([S+:41]([C:38]2[CH:39]=[CH:40][C:35]([CH3:50])=[CH:36][CH:37]=2)[C:32]2[CH:31]=[CH:30][C:29]([O:28][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])=[CH:34][CH:33]=2)=[CH:48][CH:47]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 6395Methanesulfonic AcidHCID 14812Phosphorus oxide (P4O10)HCID 15680p-Tolyl sulfoxideHCID 74558Octyl phenyl etherHCID 2724016Ammonium (1S)-[7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulphonate

Produkt 1

HCID 86761095
Di-(4-tolyl)-4-octyloxyphenylsulfonium 10-camphorsulfonate

Versuchsvorschrift

A 3-neck flask equipped with a thermometer, a nitrogen outlet and a mechanical stirrer, was charged with phosphorous pentoxide (8.64 g) followed by methanesulfonic acid (85.20 g). The resulting mixture was stirred at room temperature for 0.5 hour and then heated at 50° C. for 2-3 hours to obtain a homogeneous suspension. The mixture was cooled to below 10° C. in an ice-water bath and n-octylphenyl ether (21.66 g, 0.105 mol) was added. Next, p-tolylsulfoxide (20.03 g, 0.10 mol) was added with good stirring while maintaining the temperature of the reaction below 10° C. After stirring for 1 hour, the cooling bath was removed and the reaction was stirred at room temperature for 16 hours. Thereafter, the reaction mixture was added dropwise to a mixture of ice-water (500 mL) with vigorous stirring. The aqueous mixture was washed with toluene/hexane (3×100 mL, 1:1) and extracted with dichloromethane (3×200 mL). The combined organic layers were treated with an aqueous solution of ammonium 10-camphorsulfonate (prepared by neutralization of 10-camphorsulfonic acid (29.04 g, 0.125 mol) with ammonium hydroxide (14.53M, 8.6 mL, 0.125 mol)). The two phase solution was stirred at room temperature for 16 hours. The layers were separated and the aqueous phase extracted with dichloromethane (3×200 mL). The combined organic layers were washed with water (3×200 mL) and concentrated in vacuo to give a dark oil which solidified on standing to give a lightly colored solid @ 65 g. The solid was triturated in ether-ethylacetate for 18 hours, collected by suction filtration and dried in vacuo to provide the title compound, di-(4-tolyl)-4-octyloxyphenylsulfonium 10-camphorsulfonate, as a white solid.

Aufarbeitung

  1. customA 3-neck flask equipped with a thermometer, a nitrogen outlet and a mechanical stirrer
  2. temperatureheated at 50° C. for 2-3 hours
  3. customto obtain a homogeneous suspension
  4. temperatureThe mixture was cooled to below 10° C. in an ice-water bath
  5. stirringwith good stirring
  6. temperaturewhile maintaining
  7. customthe temperature of the reaction below 10° C
  8. stirringAfter stirring for 1 hour
  9. customthe cooling bath was removed
  10. stirringthe reaction was stirred at room temperature for 16 hours
  11. additionThereafter, the reaction mixture was added dropwise to a mixture of ice-water (500 mL) with vigorous stirring
  12. washThe aqueous mixture was washed with toluene/hexane (3×100 mL, 1:1)
  13. extractionextracted with dichloromethane (3×200 mL)
  14. stirringThe two phase solution was stirred at room temperature for 16 hours
  15. customThe layers were separated
  16. extractionthe aqueous phase extracted with dichloromethane (3×200 mL)
  17. washThe combined organic layers were washed with water (3×200 mL)
  18. concentrationconcentrated in vacuo
  19. customto give a dark oil which
  20. customto give a lightly colored solid @ 65 g
  21. customThe solid was triturated in ether-ethylacetate for 18 hours
  22. filtrationcollected by suction filtration
  23. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-196159005c054352910f2eeb2d40d99b
Quelldatensatz
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07704668B1

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