Reaktion #624754

ord-7d733c55b4ff489bbf1838aa99db69ec

Reaktionsgleichung

O=CCCC(F)(F)F
4,4,4-trifluorobutanal
CCOC(=O)c1ccc(I)cc1
ethyl 4-iodobenzoate
C[CH](C)[Mg][Cl].[Cl-].[Li+]
isopropylmagnesium chloride lithium chloride
CCOC(=O)c1ccc(C(O)CCC(F)(F)F)cc1
(+/−)-ethyl 4-(4,4,4-trifluoro-1-hydroxybutyl)benzoate

Lösungsmittel

Reaktionsbedingungen

Temperatur
-40°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added dropwise
  2. 2
    Temperaturslowly warmed to ambient temperature over 12 hours
  3. 3
    SonstigeThe reaction was quenched with aqueous 1.0M hydrochloric acid
  4. 4
    Extraktionthe aqueous layer was extracted with ethyl acetate (3×)
  5. 5
    TrocknenThe combined organic layers were dried over magnesium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated in vacuo
  8. 8
    SonstigeThe alcohol was used without further purification

Vorschrift

To a solution of the ethyl 4-iodobenzoate (1.21 ml, 7.24 mmol) in tetrahydrofuran (12 ml) at −40° C. was added isopropylmagnesium chloride lithium chloride complex (6.13 ml, 7.97 mmol, 1.3M in tetrahydrofuran) dropwise. The mixture was stirred for approximately 1 hour whereupon the 4,4,4-trifluorobutanal (0.761 ml, 0.724 mmol) was added dropwise. The mixture was stirred at −40° C. for 15 minutes and slowly warmed to ambient temperature over 12 hours. The reaction was quenched with aqueous 1.0M hydrochloric acid and the aqueous layer was extracted with ethyl acetate (3×). The combined organic layers were dried over magnesium sulfate, filtered, and concentrated in vacuo. The alcohol was used without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08859591B2uspto-grants-2014_10