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Thiophenol → 2-Chloro-4-phenylthioaniline

HRID 841190
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 841190
[Cl:1][C:2]1[CH:8]=[C:7](I)[CH:6]=[CH:5][C:3]=1[NH2:4].[C:10]1([SH:16])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C[O-].[Na+]>C(O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:1][C:2]1[CH:8]=[C:7]([S:16][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:6]=[CH:5][C:3]=1[NH2:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 7969ThiophenolHCID 2829302-Chloro-4-iodoanilineHCID 10942334Sodium Methoxide

Produkt 1

HCID 222872082-Chloro-4-phenylthioaniline

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418397HCID 178418397, VerbindungKatalysator
HCID 702
Ethanol
Lösungsmittel

Versuchsvorschrift

Tetrakis(triphenylphosphine)palladium(0) (0.1 15 g) was added to a deoxygenated mixture of 2-chloro-4-iodoaniline (0.507 g), thiophenol (0.214 ml) and sodium methoxide (0.227 g) in ethanol (20 ml). The mixture was further deoxygenated by evacuation and refilling with argon (3 cycles) then heated under reflux with stirring under argon for 18 hours, cooled, diluted with ether (30 ml) and filtered. Volatile material was removed by evaporation and the residue was purified by chromatography on a silica gel Mega Bond Elut column eluting with 10-15% ethyl acetate/hexane to give the title compound (0.443 g) as a solid. M.p. 59-60° C.; NMR: 5.78 (br s, 2H), 6.8 (t, 1H), 7.04 (m, 2H), 7.15 (m, 2H), 7.2-7.35 (m, 3H); EA: C12H10ClNS requires C, 61.1; H, 4.3; N, 5.9; S, 13.6%; found: C, 60.8; H, 4.4; N, 5.7; S, 13.3%.

Aufarbeitung

  1. customThe mixture was further deoxygenated by evacuation and refilling with argon (3 cycles)
  2. temperaturethen heated
  3. temperatureunder reflux
  4. temperaturecooled
  5. additiondiluted with ether (30 ml)
  6. filtrationfiltered
  7. customVolatile material was removed by evaporation
  8. customthe residue was purified by chromatography on a silica gel Mega Bond Elut column
  9. washeluting with 10-15% ethyl acetate/hexane

Quellen und Nachweise

ORD-Eintrag
ord-11a6c1f5558c4f74beef4f56f34e74cf
Quelldatensatz
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06369273B1

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