Reaktion #1808467

ord-3635554a77c149f9b9b46b6e1e667db9

Reaktionsgleichung

S=C(Cl)Cl
thiophosgene
CCCCC(N)CO
DL-2-amino-1-hexanol
CCN(CC)CC
triethylamine
CCCCC1COC(=S)N1
4-butyloxazolidine-2-thione

Lösungsmittel

Reaktionsbedingungen

Temperatur
20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeevaporated under reduced pressure
  2. 2
    Sonstigethe residue partitioned between water and diethylether
  3. 3
    ExtraktionThe ether extract
  4. 4
    Trocknenwas dried with sodium sulphate
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigeevaporated
  7. 7
    workup.DISSOLUTIONThe residue was dissolved in the minimum of hot 1:1 dimethylether-hexane
  8. 8
    Sonstigecrystallised
  9. 9
    Temperaturon cooling

Vorschrift

To a stirred cold solution of DL-2-amino-1-hexanol (1.1 ml) in dry THF (10 ml) was added triethylamine (2.8 ml) followed by dropwise addition of thiophosgene (0.81 ml) in dry THF (9 ml). The mixture was then stirred for 18 h at 20° C., evaporated under reduced pressure and the residue partitioned between water and diethylether. The ether extract was dried with sodium sulphate filtered and evaporated. The residue was dissolved in the minimum of hot 1:1 dimethylether-hexane and crystallised on cooling to give 4-butyloxazolidine-2-thione, mp 71°-2°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05510344uspto-grants-1996_04