Reacción #981683

ord-e1cab28451eb4c7daba2d70e2d0d1ed6

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe product was recovered in a similar manner to that
  2. 2
    Otrowas chromatographed on silica (100 g)
  3. 3
    LavadoElution with chloroform:hexane (1:5)
  4. 4
    Otroafforded unreacted
  5. 5
    Lavadowhile elution with chloroform: hexane (1:4)

Procedimiento

A solution of 1-trifluoroacetoxyadamantane (1.0 g, 4.0 mmole, prepared by reacting adamantan-1-ol with trifluoroacetic anhydride in dry pyridine) in fluorotrichloromethane (10 ml), containing m-dinitrobenzene (80 mg, 0.48 mmole), was treated with trifluoromethyl hypofluorite (4.5 mmole) at -25° for 24 hours, air being admitted to the reaction vessel during this time. The product was recovered in a similar manner to that described in Example 3 and was chromatographed on silica (100 g). Elution with chloroform:hexane (1:5) afforded unreacted starting material (152 mg), while elution with chloroform: hexane (1:4) gave liquid 3-fluoro-1-trifluoroacetoxyadamantane (489 mg) which appeared homogeneous by g.l.c. This product sublimed at 70° (bath)/1 mm Hg to give a crystalline solid m.p. 28°-32°; vmax (film) 1780 cm-1 ; PMR 1.5-2.6 (m, adamantyl protons); FMR φ*+76.2 (s, CF3COO--) and +133.5 (broad s) ppm.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04284558uspto-grants-1981_08