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Triethylamine → HCID 23501331, Verbindung

HRID 703704
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 703704
C(N(CC)CC)C.[O:8]([C:16]1[CH:17]=[C:18]([CH:23]=[CH:24][CH:25]=1)[C:19]([O:21][CH3:22])=O)[Si:9]([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10].[CH:26]12[CH2:35][CH:30]3[CH2:31][CH:32]([CH2:34][CH:28]([CH2:29]3)[C:27]1=O)[CH2:33]2>O.C1COCC1.CCCCCC.[Cl-].[Cl-].[Cl-].[Ti+3].[Zn]>[Si:9]([O:8][C:16]1[CH:17]=[C:18]([CH2:19][O:21][CH:22]=[C:27]2[CH:28]3[CH2:34][CH:32]4[CH2:31][CH:30]([CH2:35][CH:26]2[CH2:33]4)[CH2:29]3)[CH:23]=[CH:24][CH:25]=1)([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 3

HCID 8471Triethylamine2×HCID 64151AdamantanoneHCID 11715937Benzoic acid, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, methyl ester

Produkt 1

HCID 23501331HCID 23501331, VerbindungAusbeute 82,2 %

Reagenzien, Katalysatoren, Lösungsmittel 5

HCID 23994ZincKatalysator
HCID 10313229
titanium(III) trichloride
Katalysator
HCID 962WaterLösungsmittel
HCID 8028TetrahydrofuranLösungsmittel2×
HCID 8058HexaneLösungsmittel

Versuchsvorschrift

To a four-necked round-bottom flask equipped with a refluxing condenser and mechanical stirrer was added 1.5 L of dry THF under argon. Titanium trichloride (TiCl3, 200 g, 1.29 mol) was then added to the flask with stirring. After 15 minutes of stirring, powdered zinc (130 g, 2.0 mol) was added in portions and the flask was heated in hot water for 25 minutes. The reaction flask was then cooled in an ice-salt bath and the temperature of the mixture maintained at 5° to 7° C. Triethylamine (2.0 mL) was added to the suspension with caution (the reaction is extremely exothermic). The reaction started in approximately 5 to 10 minutes. After the reaction subsided, an additional amount of triethylamine (200 mL) was added and the mixture heated under reflux for 3 hours. After this period, a solution of methyl 3-tert-butyldimethylsiloxybenzoate (100 g, 0.37 mol) and 2-adamantanone (85.0 g, 0.57 mol) in 400 mL of dry THF was added dropwise to the refluxing mixture over 5 hours. The reaction mixture was then cooled to room temperature and was diluted with hexane (4 L) and the stirring continued. The suspended solids were then allowed to settle and the organic layer decanted. The black solid was washed with diethyl ether (2×1 L). Hexane (1 L) was added to the black material, followed by 1 L of water and the organic layer was removed. The aqueous layer was washed a second time with 1.5 L of hexane. The combined hexane and ether layers were then gravity filtered and the resulting solution was dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure and chromatography over silica gel with 5% ethyl acetate/hexane gave 117 g (81% yield) of 2 as a clear oil.

Aufarbeitung

  1. customTo a four-necked round-bottom flask equipped with a refluxing condenser and mechanical stirrer
  2. stirringAfter 15 minutes of stirring
  3. temperatureThe reaction flask was then cooled in an ice-salt bath
  4. temperaturethe temperature of the mixture maintained at 5° to 7° C
  5. temperaturethe mixture heated
  6. temperatureunder reflux for 3 hours
  7. waitAfter this period
  8. customthe organic layer decanted
  9. washThe black solid was washed with diethyl ether (2×1 L)
  10. additionHexane (1 L) was added to the black material
  11. customthe organic layer was removed
  12. washThe aqueous layer was washed a second time with 1.5 L of hexane
  13. filtrationgravity filtered
  14. dry with materialthe resulting solution was dried over anhydrous magnesium sulfate
  15. customEvaporation of the solvent under reduced pressure and chromatography over silica gel with 5% ethyl acetate/hexane

Quellen und Nachweise

ORD-Eintrag
ord-9dcce1f30b2d4f7e9c03dd41fa9ccbbe
Quelldatensatz
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04983779

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