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Boron trifluoride etherate → HCID 54724868, Verbindung

HRID 2293672
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2293672
[OH:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[O:5][C:4](=[O:12])[CH:3]=1.[CH:13]1([CH2:19][CH:20]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)O)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.B(F)(F)F.CCOCC>O1CCOCC1>[CH:22]1([CH2:20][CH:19]([C:3]2[C:4](=[O:12])[O:5][C:6]3[C:11]([C:2]=2[OH:1])=[CH:10][CH:9]=[CH:8][CH:7]=3)[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8000Boron trifluoride etherateHCID 15711730α-(Cyclohexylmethyl)benzenemethanolHCID 546829304-Hydroxycoumarin

Produkt 1

HCID 54724868HCID 54724868, VerbindungAusbeute 7,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

To a time-dried flask containing a mixture of 650 mg of 4-hydroxycoumarin and 1.01 g of 2-cyclohexyl-1-phenylethanol of Preparation 19 in 20 mL of dioxane under an argon atmosphere is added 2.5 mL of boron trifluoride etherate. The resulting yellow solution is left to stir at room temperature overnight. The volatiles are removed and the residue is partioned between diethyl ether and 1N sodium hydroxide. The basic aqueous phase is washed with diethyl ether and acidified to pH=l with 6N hydrochloric acid. The resulting precipitant is repeatedly extracted with dichloromethane (methanol-chloroform co-solvents). The combined dichloromethane extracts are washed once with dilute sodium bicarbonate to remove most of the unreacted 4-hydroxycoumarin, then brine, dried (magnesium sulfate), and finally concentrated under reduced pressure. The residue is adsorbed onto silica and flash column chromatographed with 30% to 60% ethyl acetate in hexanes to yield 110 mg of the title product as a tan solid.

Aufarbeitung

  1. additionTo a time-dried flask containing
  2. waitThe resulting yellow solution is left
  3. customThe volatiles are removed
  4. washThe basic aqueous phase is washed with diethyl ether
  5. extractionThe resulting precipitant is repeatedly extracted with dichloromethane (methanol-chloroform co-solvents)
  6. washThe combined dichloromethane extracts are washed once with dilute sodium bicarbonate
  7. customto remove most of the unreacted 4-hydroxycoumarin
  8. dry with materialbrine, dried (magnesium sulfate)
  9. concentrationfinally concentrated under reduced pressure
  10. customchromatographed with 30% to 60% ethyl acetate in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-af6a0468dc184e18bef6bd9192bd0557
Quelldatensatz
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05686486

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