Reaktion #53856

ord-c4a98e498ee949289813ea1eb90d0428

Reaktionsgleichung

CCN(CC)CC
triethylamine
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](C=O)CC1
trans-(4-Formyl-cyclohexyl)-methyl-carbamic acid tert-butyl ester
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
BrC(Br)(Br)Br
tetrabromomethane
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](C=C(Br)Br)CC1
trans-[4-(2,2-Dibromo-vinyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester
Ausbeute 67.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheated up
  2. 2
    Temperaturheated up
  3. 3
    Temperaturto reflux
  4. 4
    workup.ADDITIONwere added during 10 min
  5. 5
    Sonstigeevaporated
  6. 6
    Filtrationfiltered through silica gel (deactivated with hexane/Et3N) with hexane

Vorschrift

A solution of 52.45 g (200 mmol) triphenylphosphine in 200 ml CH2Cl2 was treated with 33.16 g (100 mmol) tetrabromomethane (the reaction heated up to reflux) and after 50 min with 32.06 ml (230 mmol) triethylamine (the reaction heated up to reflux and became dark violet). After cooling (0° C.), 12.83 g (50 mmol) of trans-(4-Formyl-cyclohexyl)-methyl-carbamic acid tert-butyl ester in 125 ml CH2Cl2 were added during 10 min. The solution was stirred for 16 h at RT, evaporated and filtered through silica gel (deactivated with hexane/Et3N) with hexane and then hexane/ether 4:1 to 1:1 as eluent to yield 13.28 g (67%) of trans-[4-(2,2-Dibromo-vinyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester, mp: 93-99° C., dec.; MS: 396 (MH+, 2Br).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06858651B2uspto-grants-2005_02