반응 #312280

ord-71f7ef29a27d43e28876c9581594424d

반응 방정식

C=C=CC(C)=O
pentadienone
O=c1c(-c2ccccc2)cocc1-c1ccccc1
3,5-diphenyl-4-pyrone
O=C(Cc1ccccc1)Cc1ccccc1
1,3-diphenyl-2-propanone
CCOC=O
ethyl formate
C[O-].[Na+]
sodium methoxide
O=c1cccco1
pyrone
CC(=O)[O-].[NH4+]
ammonium acetate
[Na][Na]
disodium
O=C(C(=CO)c1ccccc1)C(=CO)c1ccccc1
1,5-dihydroxy-2,4-diphenyl-1,4-pentadien-3-one
O=c1c(-c2ccccc2)c[nH]cc1-c1ccccc1
3,5-diphenyl-4(1H)-pyridone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The compounds of this invention can be prepared by various synthetic routes

실험 절차

The compounds of this invention can be prepared by various synthetic routes. Benary and Bitter, Ber. 61, 1058 (1928) taught the synthesis of an intermediate disodium salt of 1,5-dihydroxy-2,4-diphenyl-1,4-pentadien-3-one by the condensation of 1,3-diphenyl-2-propanone with ethyl formate in the presence of sodium methoxide. The intermediate pentadienone is neutralized by strong acid and forms 3,5-diphenyl-4-pyrone. Reaction of the pyrone with ammonium acetate at an elevated temperature produces 3,5-diphenyl-4(1H)-pyridone.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04235619uspto-grants-1980_11