Reaktion #56362

ord-0c5158962e0540d9b37ae10542502089

Reaktionsgleichung

CC=CC=COCC
1-ethoxy-1,3-pentadiene
CCCCOC(=O)C=O
butyl glyoxylate
CC=CC=COCC
1-ethoxy-1,3-pentadiene
CCCCOC(=O)C=O
butyl glyoxylate
Oc1ccc(O)cc1
hydroquinone
CCCCOC(=O)C1OC(OCC)C=CC1C
butyl-3-methyl-6-ethoxy-3,6-dihydro-2H-pyran-2-carboxylate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto give 28.0 g
  2. 2
    SonstigeYield

Vorschrift

Following the procedure of Example 12, a solution of 26.7 g. (0.226 mol) of 1-ethoxy-1,3-pentadiene (purity, 95%), 32.5 g. (0.25 mol) of butyl glyoxylate and 0.250 g. of hydroquinone in 250 ml. of methylene chloride was refluxed for 48 hours to give 28.0 g. of a mixture of 1-ethoxy-1,3-pentadiene and butyl glyoxylate and 20.32 g. of distilled 2H-pyran butyl ester (b1.0 =100°-110°) as an oil. Yield based on 1-ethoxy-1,3-pentadiene, 34%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04225514uspto-grants-1980_09