Reaktion #7773

ord-93b60822344942a1918edaf6b1b87f2d

Reaktionsgleichung

CCOC(C)=O
EtOAc
O=C1CCC2(CC1)OCCO2
1,4-Cyclohexanedione mono-ethylene ketal
C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
Lithium bis(trimethylsily)amide
CCOC(=O)C#N
ethyl cyanoformate
CCOC(=O)C1CC2(CCC1=O)OCCO2
8-oxo-1,4-dioxa-spiro[4.5]decane-7-carboxylic acid ethyl ester

Lösungsmittel

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITAfter 60 min
  2. 2
    workup.ADDITIONcontaining ice
  3. 3
    WaschenThe organic layer was washed with water and brine before it
  4. 4
    Sonstigewas dried
  5. 5
    Einengenconcentrated
  6. 6
    FiltrationThis crude was filtered through a plug of silica

Vorschrift

1,4-Cyclohexanedione mono-ethylene ketal (25 g) was dissolved in THF and cooled to −78° C. 1.0 M Lithium bis(trimethylsily)amide (160 mL) in THF was added dropwise. After 30 min, ethyl cyanoformate (15.9 mL) was added dropwise. After 60 min, the solution was poured into EtOAc and water containing ice. The organic layer was washed with water and brine before it was dried and concentrated. This crude was filtered through a plug of silica to give the 8-oxo-1,4-dioxa-spiro[4.5]decane-7-carboxylic acid ethyl ester (32.4 g). MS found: (M+H)+=228.9.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087604B2uspto-grants-2006_08