Boron trifluoride → 3-Carboethoxy-1,8,8-trimethylbicyclo[3,2,1]octane-2,4-dione

HRID 1940476Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1940476
[C:1]12([CH3:12])[C:9]([CH3:11])([CH3:10])[CH:6]([CH2:7][CH2:8]1)[C:4](=[O:5])[C:2]2=[O:3].[N+](=[CH:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[N-].B(F)(F)F>CCOCC>[C:16]([CH:15]1[C:4](=[O:5])[CH:6]2[C:9]([CH3:10])([CH3:11])[C:1]([CH3:12])([CH2:8][CH2:7]2)[C:2]1=[O:3])([O:18][CH2:19][CH3:20])=[O:17]

Komponenten

5

Edukt 3

HCID 6356Boron trifluorideHCID 12192Ethyl diazoacetateHCID 25208Bornane-2,3-dione

Produkt 1

HCID 189798163-Carboethoxy-1,8,8-trimethylbicyclo[3,2,1]octane-2,4-dione

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel2×

Versuchsvorschrift

To a solution of (±) camphorquinone [(1,7,7) -trimethylbicyclo[3,2,1]-heptane-2,3-dione] (15.0 g, 90.24 mmol) and ethyl diazoacetate (11.8 g, 103.7 mmol) in 120 ml of ether is added, at 0°, BF3.ether (4 ml). The mixture is stirred at RT for 24 hr. The reaction mixture is extracted with 5% K2CO3 /H2O until no polar ethyl carboxyl dione remains. The combined aqueous extracts are acidified with conc. HCl and extracted with ether. The combined organic extracts are dried and evaporated to dryness to give crystalline 3-carboethoxy-1,8,8-trimethylbicyclo[3,2,1 ]octane-2,4-dione.

Aufarbeitung

  1. extractionThe reaction mixture is extracted with 5% K2CO3 /H2O until no polar ethyl carboxyl dione
  2. extractionextracted with ether
  3. customThe combined organic extracts are dried
  4. customevaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-2cdd18bf0c834098959cbbfe3fff974c
Quelldatensatz
uspto-grants-1997_12
Patentnummer
US05700762

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