Cyclopentanethiol → Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilane

HRID 503094

Reaktionsgleichung

Reaktionsgleichung von HRID 503094
[C:1]([Si:5]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12](I)[CH:11]=1)([CH3:7])[CH3:6])([CH3:4])([CH3:3])[CH3:2].[CH:17]1([SH:22])[CH2:21][CH2:20][CH2:19][CH2:18]1>CN1CCCC1=O.C(N(CC)CC)C.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[C:1]([Si:5]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([S:22][CH:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)[CH:11]=1)([CH3:7])[CH3:6])([CH3:4])([CH3:3])[CH3:2]

Komponenten

6

Edukt 2

HCID 15510CyclopentanethiolHCID 66845200HCID 66845200, Verbindung

Produkt 1

HCID 66845801Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilaneAusbeute 82,2 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 9811564Bis(dibenzylideneacetone)palladiumKatalysatorHCID 8471TriethylamineLösungsmittelHCID 13387N-methyl-2-pyrrolidoneLösungsmittel

Versuchsvorschrift

Tert-butyl[(3-iodobenzyl)oxy]dimethylsilane (WO9513095) (1.44 g) in dry 1-methyl-2-pyrrolidone (15 ml) and triethylamine (4 ml) was stirred at room temperature under nitrogen. 1-1′Bis(diphenylphosphino)ferrocene (110 mg) and tris(dibenzylideneacetone)dipalladium(0) (258 mg) were added and the mixture was stirred for 15 min. Cyclopentyl mercaptan (0.42 g) was then added, and the reaction mixture stirred at 60° C. for 2 h. The reaction mixture was cooled to room temperature, poured onto water and extracted with diethyl ether. The combined organic extracts were dried (MgSO4) and the solvent evaporated in vacuo. The residue was purified on a 50 g SPE, eluting with a stepped gradient of 10 to 100% dichloromethane-cyclohexane to give the title compound (1.09 g) LCMS RT=4.67 min

Aufarbeitung

  1. stirringthe reaction mixture stirred at 60° C. for 2 h
  2. additionpoured onto water
  3. extractionextracted with diethyl ether
  4. dry with materialThe combined organic extracts were dried (MgSO4)
  5. customthe solvent evaporated in vacuo
  6. customThe residue was purified on a 50 g SPE
  7. washeluting with a stepped gradient of 10 to 100% dichloromethane-cyclohexane

Quellen und Nachweise

ORD-Eintrag
ord-3c1d0c72c83c4f92ade1122c2fd59647
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07776895B2

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