Carbon Dioxide → 7-(4-Methoxyphenyl)heptyl phenyl sulfide

HRID 426877Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 426877
C1([Li])C=CC=CC=1.[C:8]1([S:14][CH3:15])[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.C(=O)=O.[CH3:19][O:20][C:21]1[CH:26]=[CH:25][C:24]([CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32]I)=[CH:23][CH:22]=1>O.O1CCCC1>[C:8]1([S:14][CH2:15][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][C:24]2[CH:23]=[CH:22][C:21]([O:20][CH3:19])=[CH:26][CH:25]=2)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

Komponenten

7

Edukt 4

HCID 280Carbon DioxideHCID 7520ThioanisoleHCID 14977896HCID 14977896, VerbindungHCID 178506676HCID 178506676, Verbindung

Produkt 1

HCID 203899877-(4-Methoxyphenyl)heptyl phenyl sulfide

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

Phenyllithium (378 ml., 0.755 mole) was added over a period of 2-5 minutes to a solution of 94.5 g. of thioanisole in 600 ml. of tetrahydrofuran, stirred under nitrogen. The mixture was stirred at room temperature for about 16 hours, then cooled to -70° C. (solid CO2), and 141 g. of 6-(4-methoxyphenyl)hexyl iodide in 210 ml. of tetrahydrofuran was added slowly. The reaction mixture was stirred at -65° C. for two hours and then allowed to warm to room temperature. Water was added and the mixture extracted with pentane. The pentane extracts were washed with water, dried and concentrated to remove the solvent. The residue was distilled in vacuo, b.p. 171°-174° C. (0.15 mm.). The distillate crystallized and was recrystallized from pentane, to give 7-(4-methoxyphenyl)heptyl phenyl sulfide, m.p. 58°-59° C.

Aufarbeitung

  1. stirringThe reaction mixture was stirred at -65° C. for two hours
  2. temperatureto warm to room temperature
  3. extractionthe mixture extracted with pentane
  4. washThe pentane extracts were washed with water
  5. customdried
  6. concentrationconcentrated
  7. customto remove the solvent
  8. distillationThe residue was distilled in vacuo, b.p. 171°-174° C. (0.15 mm.)
  9. customThe distillate crystallized
  10. customwas recrystallized from pentane

Quellen und Nachweise

ORD-Eintrag
ord-04c5aa86b45945959167d1b9faf4261f
Quelldatensatz
uspto-grants-1979_10
Patentnummer
US04171378

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