Reaktion #833519

ord-a9d5174c10ce4cf9a5b16df71b64ede7

Reaktionsgleichung

CCCCCC
hexane
[Li][CH2]CCC
nBuLi
C1CCOC1
THF
CCCCCCCCCCOc1ccc(Br)cc1OCCCCCCCCCC
2a
CCCCCCCCCCOc1ccc(Br)cc1OCCCCCCCCCC
4-bromo-1,2-didecyloxybenzene
CCCCCCCCCCOc1ccc(-c2ccc(OCCCCCCCCCC)c(OCCCCCCCCCC)c2)cc1OCCCCCCCCCC
3,3′,4,4′-tetrakisdecyloxybiphenyl
Ausbeute 38.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigehad been precooled to −30° C
  2. 2
    workup.ADDITIONOnce the addition
  3. 3
    Extraktionextracted with ether
  4. 4
    WaschenThe ether layer was washed with water
  5. 5
    Trocknendried with MgSO4
  6. 6
    SonstigeThe solvent was removed under reduced pressure
  7. 7
    SonstigeThe residue was crystallized from a THF/MeOH mixture at −15° C.

Vorschrift

A hexane solution of nBuLi (1.57 M, 1.02 mL) was added dropwise to a THF solution (50 mL) of 2a which had been precooled to −30° C. Once the addition was complete the reaction mixture was allowed to warm to room temperature. After stirring for an additional 12 h the reaction mixture was poured into water and extracted with ether. The ether layer was washed with water and dried with MgSO4. The solvent was removed under reduced pressure. The residue was crystallized from a THF/MeOH mixture at −15° C. to give colorless crystals of 3,3′,4,4′-tetrakisdecyloxybiphenyl (3a) in 38% yield (mp 85-86° C.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07393503B2uspto-grants-2008_07