Water → Ethyl 8-oxo-1,4-dioxaspiro[4.5]decane-7-carboxylate

HRID 1374361

Reaktionsgleichung

Reaktionsgleichung von HRID 1374361
[H-].[Na+].[CH2:3]([O:5][C:6](=O)[O:7]CC)[CH3:4].[CH2:11]1[O:21][C:14]2([CH2:19][CH2:18][C:17](=[O:20])[CH2:16][CH2:15]2)[O:13][CH2:12]1.O>CCCCCC.C1COCC1.C(O)(=O)C>[CH2:3]([O:5][C:6]([CH:18]1[C:17](=[O:20])[CH2:16][CH2:15][C:14]2([O:13][CH2:12][CH2:11][O:21]2)[CH2:19]1)=[O:7])[CH3:4]

Komponenten

8

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Sodium hydride (60% dispersion; 45 g, 1.17 mol) was washed with 500 ml of hexane (2×), suspended in 750 mL of THF and treated with diethylcarbonate (112.5 g, 0.94 mol). The suspension was heated to reflux and treated drop-wise with a solution of 1,4-cyclohexanedione mono-ethylene ketal (60.0 g , 0.384 mol) in THF (250 mL). After the addition was complete the suspension was heated to reflux for an additional 4 hours. The mixture was cooled in an ice bath to 0° C. and then poured, while vigorously stirring, into a mixture of ice (1 L), water (100 mL) and acetic acid (100 mL). The resulting mixture was extracted with hexane (2 L total) and the extracts washed with water and brine. The hexane extract was dried over Na2SO4, filtered and concentrated to give 8-Oxo-1,4-dioxa-spiro[4.5]decane-7-carboxylic acid ethyl ester as a pale yellow oil. This was used without further purification.

Aufarbeitung

  1. temperatureThe suspension was heated
  2. temperatureto reflux
  3. additionAfter the addition
  4. temperaturewas heated
  5. temperatureto reflux for an additional 4 hours
  6. additionpoured
  7. extractionThe resulting mixture was extracted with hexane (2 L total)
  8. washthe extracts washed with water and brine
  9. extractionThe hexane extract
  10. dry with materialwas dried over Na2SO4
  11. filtrationfiltered
  12. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-dc5d2cf0cb75406e84b9a287901ddb07
Quelldatensatz
uspto-grants-2007_01
Patentnummer
US07163937B2

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