Ammonium Chloride → (3-{(1R,2S,3R)-3-(tert-Butyldimethylsilanyloxy)-2-[(S)-(E)-3-(tert-butyldimethylsilanoxy)oct-1-enyl]-5-oxocyclopentylsulfanyl} propylsulfanyl)acetic acid methyl ester

HRID 2187967Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2187967
C([Li])(C)(C)C.[C:6]([Si:10]([O:13][C@H:14](/[CH:20]=[CH:21]/I)[CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])([CH3:12])[CH3:11])([CH3:9])([CH3:8])[CH3:7].[CH3:23][O:24][C:25](=[O:46])[CH2:26][S:27][CH2:28][CH2:29][CH2:30][S:31][C:32]1[C:36](=[O:37])[CH2:35][C@@H:34]([O:38][Si:39]([C:42]([CH3:45])([CH3:44])[CH3:43])([CH3:41])[CH3:40])[CH:33]=1.[NH4+].[Cl-]>CCCCC.CCOCC.C1COCC1>[CH3:23][O:24][C:25](=[O:46])[CH2:26][S:27][CH2:28][CH2:29][CH2:30][S:31][C@H:32]1[C:36](=[O:37])[CH2:35][C@@H:34]([O:38][Si:39]([C:42]([CH3:43])([CH3:45])[CH3:44])([CH3:41])[CH3:40])[C@@H:33]1/[CH:21]=[CH:20]/[C@@H:14]([O:13][Si:10]([C:6]([CH3:7])([CH3:9])[CH3:8])([CH3:11])[CH3:12])[CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]

Komponenten

8

Edukt 4

HCID 25517Ammonium ChlorideHCID 11111369(3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octeneHCID 15406175[3-[(R)-3-(tert-Butyldimethylsilanyloxy)-5-oxocyclopent-1-enylsulfanyl]propylsulfanyl}acetic acid methyl esterHCID 178418306HCID 178418306, Verbindung

Produkt 1

HCID 12990739(3-{(1R,2S,3R)-3-(tert-Butyldimethylsilanyloxy)-2-[(S)-(E)-3-(tert-butyldimethylsilanoxy)oct-1-enyl]-5-oxocyclopentylsulfanyl} propylsulfanyl)acetic acid methyl esterAusbeute 39 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 3283Diethyl EtherLösungsmittel2×HCID 8003PentaneLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

tert-Butyllithium (1.47 mL of a 1.7M solution in pentane, 2.5 mmol) was added dropwise to a solution of tert-butyl[(S)-1-((E)-2-iodovinyl) hexyloxy]dimethylsilane 6 (462.5 mg, 1.25 mmol) in Et2O (6.0 mL) at −78° C. After stirring for 30 min lithium 2-thienylcyanocuprate (6.0 mL of a 0.25M solution in THF, 1.5 mmol) was added and the reaction was stirred an additional 30 min at −78° C. A solution of enone 5 (430 mg, 1.1 mmol) in Et2O (1 mL) was added and stirring was continued for an additional 1 h. The reaction mixture was then quickly poured into saturated aqueous NH4Cl cooled to 0° C. The mixture was extracted with EtOAc and the organic portion was washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue was quickly purified by flash column chromatography (silica gel, 100% hexane followed by 8:1 hex/EtOAc) to afford 270 mg (39%) of the above titled compound.

Aufarbeitung

  1. additionwas added
  2. stirringstirring
  3. waitwas continued for an additional 1 h
  4. temperaturecooled to 0° C
  5. extractionThe mixture was extracted with EtOAc
  6. washthe organic portion was washed with brine
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customThe residue was quickly purified by flash column chromatography (silica gel, 100% hexane followed by 8:1 hex/EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-483f5741daac46f5b3a4e88673aaa685
Quelldatensatz
uspto-grants-2002_06
Patentnummer
US06410591B1

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