Cyclobutanecarboxylic acid, 3-ethyl- → 1-(3-Ethylcyclobutyl)ethanone

HRID 1065929

Reaktionsgleichung

Reaktionsgleichung von HRID 1065929
[CH2:1]([CH:3]1[CH2:6][CH:5]([C:7]([OH:9])=O)[CH2:4]1)[CH3:2].[CH3:10][Li]>CCOCC>[C:7]([CH:5]1[CH2:4][CH:3]([CH2:1][CH3:2])[CH2:6]1)(=[O:9])[CH3:10]

Komponenten

4

Versuchsvorschrift

A solution of 6.61 g of 3-ethylcyclobutane-1-carboxylic acid, in 52 ml of distilled ether was stirred under argon at 0°. Methyllithium (85.0 ml of a 1.53 M solution in ether) was added dropwise over a 30 minute period. The reaction mixture was stirred for three hours at 25°, then quenched with 7.3 water-methanol. The layers were separated, and the aqueous layer extracted with ether. The combined organic layers were washed with brine, dried, filtered and the solvents evaporated in vacuo. The resultant oil was distilled (aspirator vacuum) to afford 5.5 g of 1-acetyl-3-ethylcyclobutane, as a clear oil (bp 64°-67°). The material had the following spectral characteristics: nmr (CDCl3)δ0.80 and 0.82 (3H total, pair of t, each J=7.0 Hz), 1.10 and 1.12 (ca. 1.5 H total, pair of s, side product 1-[2-hydroxyprop-2-yl]-3-ethylcyclobutane), 1.0-2.4 (7H, m), 2.07 and 2.09 (3H total, pair of s) and 2.7-3.5 ppm (1H, m); ir (CHCl3) 935, 1175, 1370, 1460, 1705, 2870, 2930 and 2970 cm-1, also small 3200-3600 broad and 3600 cm-1 for the side product noted above.

Aufarbeitung

  1. customquenched with 7.3 water-methanol
  2. customThe layers were separated
  3. extractionthe aqueous layer extracted with ether
  4. washThe combined organic layers were washed with brine
  5. customdried
  6. filtrationfiltered
  7. customthe solvents evaporated in vacuo
  8. distillationThe resultant oil was distilled (aspirator vacuum)

Quellen und Nachweise

ORD-Eintrag
ord-e58225b911b6476ca1cd377e6c33c14f
Quelldatensatz
uspto-grants-1982_05
Patentnummer
US04331688

Verknüpfte Notizen

Wird geladen…