Reaktion #62747

ord-aa6a6fa04b4f4744842fb2397954495f

Reaktionsgleichung

O
water
CCOC(=O)CC#N
ethylcyanoacetate
COc1cc(C=O)c2c(c1OC)OCC=C2
7,8-dimethoxy-5-formyl-2H-1-benzopyran
C1CCNCC1
piperidine
CCOC(=O)C(C#N)=Cc1cc(OC)c(OC)c2c1C=CCO2
orange solid
Ausbeute 66.9%
CCOC(=O)C(C#N)=Cc1cc(OC)c(OC)c2c1C=CCO2
Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoate
Ausbeute 66.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturto cool
  3. 3
    ExtraktionThe solution was extracted successively with water (200 mL), 0.5N hydrochloric acid (200 mL), saturated sodium bicarbonate solution (200 mL), H2O (200 mL)
  4. 4
    Trocknendried over magnesium sulfate
  5. 5
    SonstigeThe volatiles were removed under reduced pressure

Vorschrift

A mixture of ethylcyanoacetate (11.3 g, 0.1 mole), 7,8-dimethoxy-5-formyl-2H-1-benzopyran (22.0 g, 0.1 mole), piperidine (1.02 g, 0.01 mole) and acetic acid (0.36 g, 0.006 mole) in benzene (100 mL) was heated at reflux for 5 hr with azeotropic removal of water and allowed to cool. The solution was extracted successively with water (200 mL), 0.5N hydrochloric acid (200 mL), saturated sodium bicarbonate solution (200 mL), H2O (200 mL) and dried over magnesium sulfate. The volatiles were removed under reduced pressure to give 21.1 g (66.9%) of an orange solid, mp 104.5°-107.5° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04761475uspto-grants-1988_08