Reaktion #1734

ord-bec0b13badfd4aa9b7a9fafcead8a865

Reaktionsgleichung

O=C=O
CO2
[Li][CH2]CCC
nBuLi
CCCCCCc1cc2c(cc1Br)CCCCC2(C)C
2-bromo-3-hexyl-5,5-dimethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene
CCCCCCc1cc2c(cc1C(=O)O)CCCCC2(C)C
3-hexyl-5,5-dimethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene-2-carboxylic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe cooling bath was removed
  2. 2
    workup.WAITAfter 10 min.
  3. 3
    workup.ADDITIONthe mixture was poured on to ice/NH4Cl solution
  4. 4
    Extraktionextracted with diethyl ether
  5. 5
    Waschenwashed with H2O
  6. 6
    Trocknendried over Na2SO4
  7. 7
    Sonstigethe solvent was removed in a vacuum

Vorschrift

This 3.21 g of 2-bromo-3-hexyl-5,5-dimethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene were placed in 30 ml of abs. tetrahydrofuran under Ar and treated at -78° with 6.75 ml of 1.55M nBuLi (hexane) (1.1 eq.). The metal/halogen exchange was followed by gas chromatography (GC). After 40 min., a large excess of CO2 gas was introduced and the cooling bath was removed. After 10 min., the mixture was poured on to ice/NH4Cl solution, extracted with diethyl ether, washed with H2O, dried over Na2SO4 and the solvent was removed in a vacuum. Flash chromatography on SiO2 (hexane/ethyl acetate=8/2) yielded 2.26 g of 3-hexyl-5,5-dimethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene-2-carboxylic acid as white crystals of m.p. 74°-75°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726191uspto-grants-1998_03