Reacción #322786

ord-e92168529cb8454cb26c838eb4ed9cf6

Ecuación de reacción

CCCC(=O)C1=C(O)CC(c2cc(C)c3ccccc3c2C)CC1=O
2-butyryl-5-(1,4-dimethylnaphth-2-yl)-3-hydroxycyclohex-2-en-1-one
CCON.Cl
ethoxyamine hydrochloride
CC(=O)[O-].O.O.O.[Na+]
sodium acetate trihydrate
CCCC(=NOCC)C1=C(O)CC(c2cc(C)c3ccccc3c2C)CC1=O
5-(1,4-dimethylnaphth-2-yl)-2-[1-(ethoxyimino)butyl]-3-hydroxycyclohex-2-en-1-one

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ExtracciónThe mixture was then immediately extracted with ether
  2. 2
    SecadoThe dried (MgSO4)
  3. 3
    Extracciónorganic extract
  4. 4
    Otrowas evaporated

Procedimiento

A mixture of 2-butyryl-5-(1,4-dimethylnaphth-2-yl)-3-hydroxycyclohex-2-en-1-one (0.25 g), ethoxyamine hydrochloride (1.3 equiv) and sodium acetate trihydrate (1.3 equiv) were stirred in ethanol (30 ml) at room temperature for 4 hr. The mixture was then immediately extracted with ether. The dried (MgSO4) organic extract was evaporated to give 5-(1,4-dimethylnaphth-2-yl)-2-[1-(ethoxyimino)butyl]-3-hydroxycyclohex-2-en-1-one as a pale yellow oil. The product was characterized by proton nuclear magnetic resonance spectroscopy and the spectroscopic data is recorded in Table 4, Example 10.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04640708uspto-grants-1987_02